De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency.
Type: article
Authors: McFarland, R, Kirby, DM, Fowler, KJ, Ohtake, A, Ryan, MT, Amor, DJ, Fletcher, JM, Dixon, JW, Collins, FA, Turnbull, DM, Taylor, RW, Thorburn, DR
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W7075608355