Mutations in beta-myosin S2 that cause familial hypertrophic cardiomyopathy (FHC) abolish the interaction with the regulatory domain of myosin-binding protein-C (Q22008775)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in beta-myosin S2 that cause familial hypertrophic cardiomyopathy (FHC) abolish the interaction with the regulatory domain of myosin-binding protein-C |
scientific article |
Statements
Mutations in beta-myosin S2 that cause familial hypertrophic cardiomyopathy (FHC) abolish the interaction with the regulatory domain of myosin-binding protein-C (English)
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M Gruen
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M Gautel
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26 February 1999
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286
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3
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933-49
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