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

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Abstract

cytochrome c oxidase, Werdnig-Hoffman disease

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