Enhanced myosin function due to a point mutation causing a familial hypertrophic cardiomyopathy
- PMID: 10764403
- DOI: 10.1161/01.res.86.7.720
Enhanced myosin function due to a point mutation causing a familial hypertrophic cardiomyopathy
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Single-molecule mechanics of R403Q cardiac myosin isolated from the mouse model of familial hypertrophic cardiomyopathy.Circ Res. 2000 Apr 14;86(7):737-44. doi: 10.1161/01.res.86.7.737. Circ Res. 2000. PMID: 10764406
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