Log on / register
Feedback | Support | My details
The amino-acid mutational spectrum of human genetic disease.
Vitkup D, Sander C, Church GM
Genome Biol 2003, 4:R72
[Full text] [PubMed] [Related articles] [Cited on BioMed Central]


printer friendly 
to  [Help]

BioMed Central articles that cite the above article:

1.


Research article    
Prediction of disease-related mutations affecting protein localization
Laurila K, Vihinen M
BMC Genomics 2009, 10:122 (23 March 2009)
[Abstract] [Full text] [PDF] [PubMed] [Related articles]

2.


Research article    
Evolutionary analyses of KCNQ1 and HERG voltage-gated potassium channel sequences reveal location-specific susceptibility and augmented chemical severities of arrhythmogenic mutations
Jackson HA, Accili EA
BMC Evolutionary Biology 2008, 8:188 (30 June 2008)
[Abstract] [Full text] [PDF] [PubMed] [Related articles]

3.


Method    
Protein interactions in human genetic diseases
Schuster-Böckler B, Bateman A
Genome Biology 2008, 9:R9 (16 January 2008)
[Abstract] [Full text] [PDF] [PubMed] [Related articles] [Cited on BioMed Central]

4.


Research article    
Spectrum of disease-causing mutations in protein secondary structures
Khan S, Vihinen M
BMC Structural Biology 2007, 7:56 (29 August 2007)
[Abstract] [Full text] [PDF] [PubMed] [Related articles] [Cited on BioMed Central]

5.


Methodology article    
Predicting deleterious nsSNPs: an analysis of sequence and structural attributes
Dobson RJ, Munroe PB, Caulfield MJ, Saqi MAS
BMC Bioinformatics 2006, 7:217 (21 April 2006)
[Abstract] [Full text] [PDF] [PubMed] [Related articles] [Cited on BioMed Central]


This article is also cited by a further 10 articles in PubMed Central


You can also check ISI Web of Science for additional citations (subscription required)
printer friendly 
to  [Help]

© 1999-2009 BioMed Central Ltd unless otherwise stated. Part of Springer Science+Business Media.