Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
Details
Original language | English |
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Pages (from-to) | 3025-3035 |
Journal | Human Molecular Genetics |
Volume | 10 |
Publication status | Published - 2001 |
Peer-reviewed | Yes |
External IDs
Scopus | 0035894664 |
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