A novel mutation in the SCO2 gene in a patient with cytochrome c oxidase deficiency and a Werdnig-Hoffmann disease phenotype | Charles Explorer

A novel mutation in the SCO2 gene in a patient with cytochrome c oxidase deficiency and a Werdnig-Hoffmann disease phenotype

Publikace

Abstrakt

cytochrome c oxidase deficiency, Werdnig-Hoffmann disease

Osoby