Open Access Highly Accessed Research article

Reassessing the role of mitochondrial DNA mutations in autism spectrum disorder

Vanesa Álvarez-Iglesias1, Ana Mosquera-Miguel1, Ivón Cuscó23, Ángel Carracedo134, Luis Alberto Pérez-Jurado2356 and Antonio Salas1*

Author Affiliations

1 Unidade de Xenética, Instituto de Medicina Legal and Departamento de Anatomía Patolóxica e Ciencias Forenses, Facultade de Medicina, Universidade de Santiago de Compostela, Galicia, Spain

2 Unidad de Genética, Universitat Pompeu Fabra, Barcelona, Spain

3 CIBER de enfermedades raras (CIBERER), Spain

4 Fundación Pública Galega de Medicina Xenómica, SERGAS, Santiago de Compostela, Galicia, Spain

5 Programa de Medicina Molecular y Genética, Hospital Universitari Vall d'Hebron, Barcelona, Spain

6 Dept. of Genome Sciences, University of Washington, Seattle, WA, USA

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BMC Medical Genetics 2011, 12:50  doi:10.1186/1471-2350-12-50

Published: 6 April 2011

Additional files

Additional file 1:

Table S1. MtDNA control sequences and coding region mtSNP genotypes. Mutations are referred to with respect to the rCRS. Transitions are omitted while transversions are indicated as a suffix. A "+" indicates an insertion whereas "del" refers to a deletion. See text for hg assignation criteria.

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