Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency (Q24317097)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency |
scientific article |
Statements
Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency (English)
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Scot C Leary
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Guy-Hellen Guercin
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Jeffrey N Agar
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Nancy G Kennaway
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Cary O Harding
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Michaela Jaksch
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Eric A Shoubridge
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15 October 2003
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12
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20
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2693-702
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