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Mutations of the SCO1 Gene in Mitochondrial Cytochrome c Oxidase Deficiency with Neonatal-Onset Hepatic Failure and Encephalopathy

✍ Scribed by Isabelle Valnot; Sandrine Osmond; Nadine Gigarel; Blandine Mehaye; Jeanne Amiel; Valérie Cormier-Daire; Arnold Munnich; Jean-Paul Bonnefont; Pierre Rustin; Agnès Rötig

Book ID: 117012770
Publisher: American Society of Human Genetics
Year: 2000
Tongue: English
Weight: 250 KB
Volume: 67
Category: Article
ISSN: 0002-9297
DOI: 10.1016/s0002-9297(07)62940-1

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