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C Paret

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Human Molecular Genetics|December 26, 2001
Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblastsM Jaksch, C Paret, R Stucka, et al.
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Showing results (11-20 of 11) with videos related to

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Pageof 2
You have reached the last page of results.This site can display upto 11 results.
Human Molecular Genetics|December 26, 2001
Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblastsM Jaksch, C Paret, R Stucka, et al.
Pageof 2