NDUFA10
References
NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease. Hoefs SJ, van Spronsen FJ, Lenssen EW, Nijtmans LG, Rodenburg RJ, Smeitink JA, van den Heuvel LP. Eur J Hum Genet. 2011 Mar;19(3):270-4. PMID: #21150889#