Conference Proceedings

De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency.

R McFarland, DM Kirby, KJ Fowler, A Ohtake, MT Ryan, DJ Amor, JM Fletcher, JW Dixon, FA Collins, DM Turnbull, RW Taylor, DR Thorburn

AMERICAN JOURNAL OF HUMAN GENETICS | UNIV CHICAGO PRESS | Published : 2003