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Open Access Research article

The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study

Jeanne C Latourelle1*, Mei Sun2, Mark F Lew3, Oksana Suchowersky4, Christine Klein5, Lawrence I Golbe6, Margery H Mark6, John H Growdon7, G Frederick Wooten8, Ray L Watts9, Mark Guttman10, Brad A Racette11, Joel S Perlmutter11, Anwar Ahmed12, Holly A Shill13, Carlos Singer14, Stefano Goldwurm15, Gianni Pezzoli15, Michela Zini15, Marie H Saint-Hilaire1, Audrey E Hendricks116, Sally Williamson1, Michael W Nagle1, Jemma B Wilk1, Tiffany Massood1, Karen W Huskey1, Jason M Laramie1, Anita L DeStefano116, Kenneth B Baker17, Ilia Itin17, Irene Litvan18, Garth Nicholson19, Alastair Corbett19, Martha Nance20, Edward Drasby21, Stuart Isaacson22, David J Burn23, Patrick F Chinnery24, Peter P Pramstaller25, Jomana Al-hinti26, Anette T Moller27, Karen Ostergaard27, Scott J Sherman28, Richard Roxburgh29, Barry Snow29, John T Slevin30, Franca Cambi30, James F Gusella2 and Richard H Myers1

Author Affiliations

1 Department of Neurology, Boston University School of Medicine, Boston University, Boston, MA, USA

2 Molecular Neurogenetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, Harvard Medical School Boston, MA, USA

3 Department of Neurology, University of Southern California, Los Angeles, CA, USA

4 Departments of Clinical Neurosciences and Medical Genetics, University of Calgary, Calgary, Alberta, Canada

5 Department of Neurology, Medical University of Lübeck, Lübeck, Germany

6 Department of Neurology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, New Brunswick, NJ, USA

7 Department of Neurology, Massachusetts General Hospital, Harvard Medical School Boston, MA, USA

8 Department of Neurology, University of Virginia Health System, Charlottesville, VA, USA

9 Department of Neurology, University of Alabama at Birmingham, Birmingham, AL, USA

10 Department of Medicine, University of Toronto, Toronto, Canada

11 Department of Neurology, Washington University School of Medicine, Saint Louis, MO, USA

12 Barrow Neurological Institute, Phoenix, AZ, USA

13 Sun Health Research Institute, Sun City, AZ, USA

14 Department of Neurology, University of Miami, Miami, FL, USA

15 Parkinson Institute, Istituti Clinici di Perfezionamento, Milano, Italy

16 Department of Biostatistics, Boston University School of Medicine, Boston University, Boston, MA, USA

17 Departments of Neurology and Neuroscience, Cleveland Clinic Foundation, Cleveland, OH, USA

18 Department of Neurology, University of Louisville School of Medicine, Louisville, KY, USA

19 Neurology Department, University of Sydney ANZAC Research Institute, Concord Hospital, Sydney, Australia

20 Struthers Parkinson's Center, Park Nicollet Clinic, Golden Valley, MN, USA

21 Port City Neurology, Scarborough, ME, USA

22 Parkinson's Disease and Movement Disorder Center of Boca Raton, Boca Raton, FL, USA

23 Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne, UK

24 Regional Neurosciences Centre, Newcastle University, Newcastle upon Tyne, UK

25 Department of Neurology, General Regional Hospital Bolzano, Bolzano, Italy

26 Department of Neurology, University of Arkansas for Medical Sciences, AR, USA

27 Department of Neurology, Aarhus University Hospital, Aarhus, Denmark

28 Department of Neurology, University of Arizona, Tucson, AZ, USA

29 Department of Neurology, Auckland City Hospital, Auckland, New Zealand

30 Department of Neurology, University of Kentucky College of Medicine, Lexington, KY, USA

For all author emails, please log on.

BMC Medicine 2008, 6:32  doi:10.1186/1741-7015-6-32


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1741-7015/6/32


Received:8 September 2008
Accepted:5 November 2008
Published:5 November 2008

© 2008 Latourelle et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

We report age-dependent penetrance estimates for leucine-rich repeat kinase 2 (LRRK2)-related Parkinson's disease (PD) in a large sample of familial PD. The most frequently seen LRRK2 mutation, Gly2019Ser (G2019S), is associated with approximately 5 to 6% of familial PD cases and 1 to 2% of idiopathic cases, making it the most common known genetic cause of PD. Studies of the penetrance of LRRK2 mutations have produced a wide range of estimates, possibly due to differences in study design and recruitment, including in particular differences between samples of familial PD versus sporadic PD.

Methods

A sample, including 903 affected and 58 unaffected members from 509 families ascertained for having two or more PD-affected members, 126 randomly ascertained PD patients and 197 controls, was screened for five different LRRK2 mutations. Penetrance was estimated in families of LRRK2 carriers with consideration of the inherent bias towards increased penetrance in a familial sample.

Results

Thirty-one out of 509 families with multiple cases of PD (6.1%) were found to have 58 LRRK2 mutation carriers (6.4%). Twenty-nine of the 31 families had G2019S mutations while two had R1441C mutations. No mutations were identified among controls or unaffected relatives of PD cases. Nine PD-affected relatives of G2019S carriers did not carry the LRRK2 mutation themselves. At the maximum observed age range of 90 to 94 years, the unbiased estimated penetrance was 67% for G2019S families, compared with a baseline PD risk of 17% seen in the non-LRRK2-related PD families.

Conclusion

Lifetime penetrance of LRRK2 estimated in the unascertained relatives of multiplex PD families is greater than that reported in studies of sporadically ascertained LRRK2 cases, suggesting that inherited susceptibility factors may modify the penetrance of LRRK2 mutations. In addition, the presence of nine PD phenocopies in the LRRK2 families suggests that these susceptibility factors may also increase the risk of non-LRRK2-related PD. No differences in penetrance were found between men and women, suggesting that the factors that influence penetrance for LRRK2 carriers are independent of the factors which increase PD prevalence in men.

Background

Parkinson's disease (PD) is a neurodegenerative disorder, affecting approximately 1.8% of individuals over the age of 65 [1]. Some cases of PD are due to known genetic or environmental factors but most are likely due to complex interactions among unidentified genes and environmental risk factors. These susceptibility factors may also play a role in the penetrance of known PD genes.

Mutations in the leucine-rich repeat kinase 2 gene (LRRK2) are the most common known genetic cause of PD. The most frequent LRRK2 mutation, G2019S, is estimated to be associated with 5% to 6% of familial PD and 1% to 2% of idiopathic cases in populations of European descent [2,3]. More than 20 additional rare mutations throughout the LRRK2 gene have been reported with varying frequency among different populations [2].

Studies of the G2019S mutation have reported a wide range of penetrance estimates. Early studies, performed in large families with multiple affected members, reported high lifetime penetrance for LRRK2 mutations, ranging from 70% [4] to 100% [5]. Subsequent studies of the age-dependent penetrance of G2019S mutations in families with multiple affected members have reported a range of penetrance estimates. Kachergus and colleagues [6] reported 17% penetrance at age 50 increasing to 85% at age 70 in 13 families segregating the G2019S mutation, while Lesage and colleagues [7] reported 33% penetrance at age 50, increasing to 100% at age 75 in 13 French and North African families ascertained for dominantly inherited PD.

More recent studies have screened ethnically diverse PD populations, who were not ascertained for familial history of the disease. These studies have generally reported lower lifetime penetrance estimates for the G2019S mutation, ranging from 22% to 32% [8-10], and decreased age-dependent penetrance ranging from 2% at age 50 to 33% at age 80 [11]. One possible explanation for the higher penetrance estimates reported among the family-based LRRK2 studies is an ascertainment bias created by more ready ascertainment of families with multiple affected members. Alternatively, genetic or environmental susceptibility factors shared by affected family members may also increase penetrance in some families.

In this study, we report age-dependent penetrance estimates for LRRK2 derived from a large sample of familial PD with consideration of the potential for bias inherent in a familial sample. Penetrance was estimated for families with either the G2019S or R1441C mutations, as well as for the G2019S mutation alone.

Methods

Subjects

Study participants were recruited by the GenePD study, an international multi-site study of the genetics of PD, using three ascertainment strategies: 1) PD-affected probands with a PD-affected sibling; 2) PD-affected probands with a PD-affected parent or offspring; and 3) PD-affected probands with another PD-affected relative such as a cousin, aunt or uncle. Both affected and unaffected relatives of the proband were recruited (Table 1). An additional series of 126 randomly ascertained PD cases was recruited through the BUMC/BU Neurology Associates clinic. Controls were recruited from the spouses or in-laws of PD patients at BUMC/BU Neurology Associates clinic and from four GenePD study site clinics. All participants gave informed consent and the study was approved by the Boston University Medical Center Institutional Review Board.

Table 1. Distribution by sex and mean ages of onset or enrollment for the idiopathic Parkinson's disease (PD), familial PD, unaffected PD relative and controls samples

The diagnostic criteria for PD affection follow the United Kingdom Brain Bank criteria, and all probands were examined by a neurologist trained as a movement disorder specialist. When possible, the affection status of other family members was also confirmed by neurological examination. In cases where examination was not possible (for example, where the affected family member was deceased) PD affection status was determined through administration of a diagnostic questionnaire (adapted from Marder et al, estimated sensitivity = 95.5% and specificity = 96.2% [12]). Family history data was collected in a structured interview which collected information on the onset age and PD affection status for all first-degree relatives of the proband.

Genotyping

Genotyping of the G2019S, R1441C, R1441H, Y1699C and I2020T mutations was performed using TaqMan technology implemented on the ABI PRISM® 7900 HT Sequence Detection system (Applied Biosystems: Foster City, CA) for 650 familial PD cases, 126 randomly ascertained PD cases, 125 controls and 30 unaffected relatives of familial PD cases. The mutations G2019S and R1441C, the only mutations observed in the initial sample size above, were typed in an additional 253 familial PD cases, 72 controls and 28 unaffected relatives of familial PD cases.

All variants identified by allelic discrimination assays were further confirmed by directly sequencing PCR products, which was performed by the DNA sequencing core at Massachusetts General Hospital using an ABI377/XL or an ABI3730 DNA analyzer. Forward and reverse primers were used with Applied Biosystems BigDye terminator v3.1 sequencing chemistry according to the manufacturer's protocol.

Estimation of penetrance

Family history data for PD affection, age at onset and age at death were used to assess penetrance among the parents of sibships ascertained for at least two PD-affected siblings where at least one of these was determined to be a LRRK2 carrier. Only the parents from families ascertained as affected sibling pairs were used in this analysis, in order to avoid bias towards increased penetrance among those families ascertained as PD-affected parent-offspring pairs. Similarly, the siblings in these sibships themselves were not used in the assessment of penetrance, in order to avoid the bias of ascertainment of sibships with multiple affected members. The parents of PD-affected siblings were used to provide an unbiased sample in which to estimate penetrance because the likelihood of PD-affected siblings being ascertained into the study is independent of the affection status of their parents.

Penetrance estimates were made under the assumption that only one parent from each LRRK2 sibship was a carrier. Because nearly all the parents were deceased, it was not possible to determine which parent was the mutation carrier. Thus, one parent per sibship was selected as the LRRK2-carrying parent using the following criteria. In families where neither parent was PD-affected, one parent was selected at random. When one parent was PD-affected, selection was weighted to select the affected parent 98.5% of the time and the unaffected parent 1.5% of the time, to allow for the presence of PD phenocopies among affected parents. This weighting was derived from a conservative estimate of an underlying population prevalence of PD of 1.5% for the age range of the study sample. This selection process was repeated 1000 times, each time randomly selecting one LRRK2 carrier parent according to the above criteria, to produce a distribution of survival estimates for PD. Final penetrance estimates were the average of the 1000 penetrance estimates.

The PROC LIFETEST procedure in SAS v9.1 was used to produce the product-limit survival estimates for each event (for example PD onset) or censoring age. Penetrance was calculated for each age by subtracting the survival estimate from 1. The same estimation was performed in the set of non-LRRK2 carrying families ascertained as affected sibling pairs to permit a comparison of the age-dependent penetrance of LRRK2 families with the age-dependent risk of PD in families of unspecified etiology.

Differences in LRRK2 penetrance by sex were examined by testing the homogeneity of the survival curves for men and women using the Log-rank test for each of the 1000 randomly selected samples.

Results

From the 903 familial PD cases studied, 58 LRRK2 mutation carriers (6.4%) were identified in 31 apparently unrelated families (Table 2). Four R1441C mutation carriers were identified in two families, while the remaining 54 carriers had G2019S mutations. Six G2019S mutations were identified in the 126 randomly ascertained PD cases (4.8%). No mutations were identified among the controls or unaffected relatives of PD cases. Nine PD-affected relatives of G2019S carriers did not carry the LRRK2 mutation themselves, suggesting that some multiplex families have multiple sources of PD and that PD phenocopies are found among LRRK2 families.

Table 2. Subjects are presented according to the method of ascertainment, with the number of unaffected relatives genotyped for LRRK2 mutations shown in parenthesis

The majority of families in this study were recruited as affected sibling pairs (401 of 509 families or 79%), and 6% of these were LRRK2 families (Table 2). Comparatively, 8% of the affected parent-offspring-ascertained families were LRRK2 families and none of the families ascertained through more distantly related affected relative pairs included LRRK2 carriers.

The average ages of onset of PD in LRRK2 carriers and non-carriers are shown in Table 3. There were no significant differences in onset age between LRRK2 carriers and non-carriers, between carriers of different types of LRRK2 mutations, or between men and women.

Table 3. Mean onset ages stratified by LRRK2 mutations and sex are shown

Family history data from 22 of the 24 families carrying LRRK2 mutations and 340 of the 377 of non-LRRK2 families ascertained through the affected sibling pair method was available for estimation of penetrance of the LRRK2 mutations. Age-dependent penetrance was estimated in 22 of 24 families carrying LRRK2 mutations ascertained through the affected sibling pair method and separately in 20 of the 22 families carrying the G2019S data (two families had incomplete family history data). The two families carrying the R1441C mutation were not analyzed separately due to the small sample size. The age -dependent penetrance of PD among the parents of non-LRRK2 families ascertained by the affected sibling pair method was estimated to provide a baseline risk for comparison.

The median, quartiles and 5th and 95th percentile of the penetrance calculated in 1000 random selections of a single parent from each G2019S family are shown in Figure 1. In order to provide a baseline for comparison, the age-dependent risk of PD in parents of non-LRRK2 PD-affected siblings is also shown. In the age range of 50 to 54, the median estimated penetrance is 10% among the G2019S carriers, compared with 1% in non-LRRK2 carriers. At the maximum observed onset age range (90 to 94 years), the median estimated penetrance reaches 67% for the parents in G2019S mutation families, approximately four times greater than the expected risk in parents of non-LRRK2 PD-affected siblings. Including the R1441C families (data not shown) increases the maximum observed penetrance to 70%.

thumbnailFigure 1. The box plot shows the median and 25th and 75th percentiles with whiskers extending to the 5th and 95th percentiles of the penetrance at each age range for G2019S carriers and for non-LRRK2 carriers among families recruited for at least two Parkinson's disease-affected siblings.

There was no observed difference in penetrance between fathers and mothers; none of the 1000 log-rank tests showed a significant difference in penetrance by sex (data not shown).

Discussion

LRRK2 mutations were identified in both randomly ascertained idiopathic PD cases and in families with multiple PD-affected members. As expected, LRRK2 mutations were more common among families with multiple cases of PD than in randomly ascertained cases and more common in families recruited as parent-offspring pairs with an apparent dominant transmission than in those recruited as affected sibling pairs. The number of mutations identified in cases with no family or parental history of PD (4.8%) is consistent with previous reports of G2019S LRRK2 mutations.

The R1441C mutation was only observed in two sets of siblings, both of whom reported a parental history of PD and at least one other PD-affected relative. While this pattern of affection is suggestive of full penetrance for this mutation, the sample is too small to justify this inference with confidence. Future studies of a larger group of R1441C and other LRRK2 mutations may provide interesting insights into the mechanisms of LRRK2-related PD through comparison of the age-dependent penetrance among the different LRRK2 mutations and their modifiers.

The more common G2019S mutation shows reduced penetrance in this sample of familial PD. However the penetrance estimated here, in a sample composed entirely of familial PD, is substantially higher than that reported previously in a sample of randomly ascertained idiopathic PD cases (67% versus 33% at age 85 [11]). Conversely, studies of G2019S in large familial samples [4-7] report higher penetrance (70 to 100% at age 75) than the 67% at age 85 reported here. Contrasting penetrance in families selected to include multiple affected members (for example 'familial PD') with penetrance in families with a single affected member (for example 'sporadic' or 'idiopathic' PD) will, by definition, generate lower estimates in the latter group if the multiple affected members required for selection in the former group are included in the estimates. We sought to avoid this bias towards inflated penetrance by studying only the parents of subjects who were recruited as sibling pairs. Nonetheless, the comparison of estimates across these different study designs indicates variability in LRRK2 penetrance among families. This suggests the presence of other genetic factors which modify the actions of LRRK2 mutations and influence the penetrance. Mutations in LRRK2 have been associated with not only typical PD but with other pathologies as well [3]. The questionnaires used for this study do encompass other disorders but are most specifically designed to identify likely PD cases. Therefore these estimates should be considered only as estimates of the penetrance of typical PD and may underestimate the penetrance of any manifestation of LRRK2-related pathology.

A positive family history of PD is associated with increased risk of PD [13] and the 17% risk among parents of PD sibling pairs in non-LRRK2 families is higher than the risk expected in the general population (see Figure 1). Genetic factors which influence the penetrance of LRRK2 mutations may either interact only with that gene or may be factors which influence the susceptibility to familial PD among non-LRRK2 carriers as well. The presence of nine phenocopies identified among the relatives of G2019S carriers suggests that at least some genetic susceptibility factors are common to both LRRK2 and non-LRRK2-related PD.

No significant difference in penetrance was seen between fathers and mothers, although men are at a generally higher risk of PD than women [14]. This suggests the possibility that modifiers of LRRK2 penetrance are independent from the sex-dependent modifiers of PD risk in general. Similarly however, no significant difference in penetrance was seen between fathers and mothers of the affected sibling pairs of non-LRRK2 families, which is more surprising, given that this sample is predominantly male (see Table 3). These two findings suggest that sex-dependent modifiers of PD risk may have a reduced effect in both LRRK2 and non-LRRK2-related familial PD, relative to that seen in sporadic or idiopathic PD. This is consistent with a recent study in a large Ashkenazi sample which also suggested that the risk of LRRK2-related PD is similar in men and women as opposed to the risk of idiopathic PD which was increased in men [15].

Conclusion

While the PD penetrance estimate of 67% for LRRK2 mutation families is four times that seen in non-LRRK2-related PD families, these studies suggest that there is a significant level of non-penetrance among LRRK2 carriers. Additionally, the presence of phenocopies and the increased penetrance in PD families compared with randomly ascertained PD samples suggest genetic susceptibility factors which affect risk of both LRRK2-related and idiopathic PD. Thus, identification of the factors which influence penetrance may hasten discovery of disease-modifying factors in both LRRK2 families as well as in idiopathic PD.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

JCL participated in the study design, recruited study subjects, performed the statistical analysis and drafted the manuscript. MS performed sequencing and reviewed the initial manuscript. MFL, OS, CK, LIG, MHM, JHG, GFW, RW, MG, BAR, JSP, AA, HAS, CS, SG, GP, MZ, MSM, KBB, II, IL, GN, AC, MN, ED, SI, DJB, PFC, PPP, JA, ATM, KO, SJS, RR, BS, JTS and FC recruited study subjects and reviewed the initial manuscript. AEH, JBW, JML, ALD, JFG participated in study design and reviewed the initial manuscript. SW and MWN performed genotyping and reviewed the initial manuscript. TM and KWH recruited study participants, participated in the coordination of the study and reviewed the initial manuscript. RHM participated in the design and coordination of the study and in drafting the manuscript. All authors read and approved the final manuscript.

Acknowledgements

This study was supported by the Bumpus Foundation, and PHS grant R01 NS36711-09 'Genetic Linkage Study in PD'. The DNA samples contributed by the Parkinson Institute – Istituti Clinici di Perfezionamento, Milan, Italy, were from the 'Human genetic bank of patients affected by PD and Parkinsonisms', supported by Italian Telethon grant n. GTF04007.

References

  1. Mayeux R: Epidemiology of neurodegeneration.

    Annual review of neuroscience 2003, 26:81-104. PubMed Abstract | Publisher Full Text OpenURL

  2. Tan EK, Skipper LM: Pathogenic mutations in Parkinson disease.

    Human mutation 2007, 28(7):641-653. PubMed Abstract | Publisher Full Text OpenURL

  3. Singleton AB: Altered alpha-synuclein homeostasis causing Parkinson's disease: the potential roles of dardarin.

    Trends in neurosciences 2005, 28(8):416-421. PubMed Abstract | Publisher Full Text OpenURL

  4. Funayama M, Hasegawa K, Kowa H, Saito M, Tsuji S, Obata F: A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.

    Annals of neurology 2002, 51(3):296-301. PubMed Abstract | Publisher Full Text OpenURL

  5. Paisan-Ruiz C, Jain S, Evans EW, Gilks WP, Simon J, Brug M, Lopez de Munain A, Aparicio S, Gil AM, Khan N, Johnson J, Martinez JR, Nicholl D, Carrera IM, Pena AS, de Silva R, Lees A, Marti-Masso JF, Perez-Tur J, Wood NW, Singleton AB: Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease.

    Neuron 2004, 44(4):595-600. PubMed Abstract | Publisher Full Text OpenURL

  6. Kachergus J, Mata IF, Hulihan M, Taylor JP, Lincoln S, Aasly J, Gibson JM, Ross OA, Lynch T, Wiley J, Payami H, Nutt J, Maraganore DM, Czyzewski K, Styczynska M, Wszolek ZK, Farrer MJ, Toft M: Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.

    American journal of human genetics 2005, 76(4):672-680. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  7. Lesage S, Ibanez P, Lohmann E, Pollak P, Tison F, Tazir M, Leutenegger AL, Guimaraes J, Bonnet AM, Agid Y, Durr A, Brice A: G2019S LRRK2 mutation in French and North African families with Parkinson's disease.

    Annals of neurology 2005, 58(5):784-787. PubMed Abstract | Publisher Full Text OpenURL

  8. Ferreira JJ, Guedes LC, Rosa MM, Coelho M, van Doeselaar M, Schweiger D, Di Fonzo A, Oostra BA, Sampaio C, Bonifati V: High prevalence of LRRK2 mutations in familial and sporadic Parkinson's disease in Portugal.

    Mov Disord 2007, 22(8):1194-1201. PubMed Abstract | Publisher Full Text OpenURL

  9. Clark LN, Wang Y, Karlins E, Saito L, Mejia-Santana H, Harris J, Louis ED, Cote LJ, Andrews H, Fahn S, Waters C, Ford B, Frucht S, Ottman R, Marder K: Frequency of LRRK2 mutations in early- and late-onset Parkinson disease.

    Neurology 2006. OpenURL

  10. Ozelius LJ, Senthil G, Saunders-Pullman R, Ohmann E, Deligtisch A, Tagliati M, Hunt AL, Klein C, Henick B, Hailpern SM, Lipton RB, Soto-Valencia J, Risch N, Bressman SB: LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

    The New England journal of medicine 2006, 354(4):424-425. PubMed Abstract | Publisher Full Text OpenURL

  11. Goldwurm S, Zini M, Mariani L, Tesei S, Miceli R, Sironi F, Clementi M, Bonifati V, Pezzoli G: Evaluation of LRRK2 G2019S penetrance: relevance for genetic counseling in Parkinson disease.

    Neurology 2007, 68(14):1141-1143. PubMed Abstract | Publisher Full Text OpenURL

  12. Marder K, Levy G, Louis ED, Mejia-Santana H, Cote L, Andrews H, Harris J, Waters C, Ford B, Frucht S, Fahn S, Ottman R: Accuracy of family history data on Parkinson's disease.

    Neurology 2003, 61(1):18-23. PubMed Abstract | Publisher Full Text OpenURL

  13. Rocca WA, McDonnell SK, Strain KJ, Bower JH, Ahlskog JE, Elbaz A, Schaid DJ, Maraganore DM: Familial aggregation of Parkinson's disease: The Mayo Clinic family study.

    Annals of neurology 2004, 56(4):495-502. PubMed Abstract | Publisher Full Text OpenURL

  14. Bower JH, Maraganore DM, McDonnell SK, Rocca WA: Incidence and distribution of parkinsonism in Olmsted County, Minnesota, 1976–1990.

    Neurology 1999, 52(6):1214-1220. PubMed Abstract | Publisher Full Text OpenURL

  15. Orr-Urtreger A, Shifrin C, Rozovski U, Rosner S, Bercovich D, Gurevich T, Yagev-More H, Bar-Shira A, Giladi N: The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect?

    Neurology 2007, 69(16):1595-1602. PubMed Abstract | Publisher Full Text OpenURL

Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1741-7015/6/32/prepub