Title: | A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia |
Journal : | American Journal of Medical Genetics Part A, 143A, 1 |
Authors: | Sarzi E ; Brown MD ; Lebon S ; Chrétien D ; Munnich A ; Rotig A ; Procaccio V |
Material Type: | Article |
Publication Date: | 2007 |
Size: | p 33 |
Languages: | English |
Pubmed / DOI : | Pubmed : 17152068 / DOI : 10.1002/ajmg.a.31565 |