Jaksch,
Paret,
Stucka,
Horn,
Müller-Höcker,
Horvath,
Trepesch,
Stecker,
Freisinger,
Thirion,
Müller,
Lunkwitz,
Rödel,
Shoubridge,
Lochmüller,
- Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts. Jaksch, M., Paret, C., Stucka, R., Horn, N., Müller-Höcker, J., Horvath, R., Trepesch, N., Stecker, G., Freisinger, P., Thirion, C., Müller, J., Lunkwitz, R., Rödel, G., Shoubridge, E.A., Lochmüller, H. Hum. Mol. Genet. (2001)