Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency (Q28140889)
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scientific article (publication date: 22 March 2000)
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency |
scientific article (publication date: 22 March 2000) |
Statements
Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency (English)
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22 March 2000
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9
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795-801
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5
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