Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency-Reference-Cited by-同舟云学术

Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency

Published:2005-08-15 Issue:18 Volume:14 Page:2737-2748
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Diaz Francisca,Thomas Christine K.,Garcia Sofia,Hernandez Dayami,Moraes Carlos T.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/14/18/2737/6949351/ddi307.pdf

Reference42 articles.

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3. Comi, G.P., Strazzer, S., Galbiati, S. and Bresolin, N. ( 2002 ) Cytochrome c oxidase deficiency. Int. Rev. Neurobiol. , 53 , 205 –240.

4. Yoshikawa, S. ( 1997 ) Beef heart cytochrome c oxidase. Curr. Opin. Struct. Biol. , 7 , 574 –579.

5. Anderson, S., Bankier, A.T., Barrell, B.G., de Bruijn, M.H., Coulson, A.R., Drouin, J., Eperon, I.C., Nierlich, D.P., Roe, B.A., Sanger, F. et al. ( 1981 ) Sequence and organization of the human mitochondrial genome. Nature , 290 , 457 –465.

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