论文信息 - Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease. - 字舞流文

Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease.

S. Dimauro | E. Schon | P. Canoll | L. Salviati | A. Hays | S. Sacconi | E. Bonilla | S. Shanske | D. Kronn | M. Davidson | A. Braun | Minerva M Rasalan