Cytochrome C oxidase deficiency in a girl with the Werdnig-Hoffman disease and a novel mutation 1518DELA in SCO2 gene | Charles Explorer

Cytochrome C oxidase deficiency in a girl with the Werdnig-Hoffman disease and a novel mutation 1518DELA in SCO2 gene

Publikace

Abstrakt

cytochrome c oxidase, Werdnig-Hoffman disease

Osoby