Author:
Swalwell Helen,Kirby Denise M,Blakely Emma L,Mitchell Anna,Salemi Renato,Sugiana Canny,Compton Alison G,Tucker Elena J,Ke Bi-Xia,Lamont Phillipa J,Turnbull Douglass M,McFarland Robert,Taylor Robert W,Thorburn David R
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference51 articles.
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4. Moreadith RW, Batshaw ML, Ohnishi T et al: Deficiency of the iron-sulfur clusters of mitochondrial reduced nicotinamide-adenine dinucleotide-ubiquinone oxidoreductase (complex I) in an infant with congenital lactic acidosis. J Clin Invest 1984; 74: 685–697.
5. Robinson BH, McKay N, Goodyer P, Lancaster G : Defective intramitochondrial NADH oxidation in skin fibroblasts from an infant with fatal neonatal lacticacidemia. Am J Hum Genet 1985; 37: 938–946.
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