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Enhanced myosin function due to a point mutation causing a familial hypertrophic cardiomyopathy

R L Moss1, J S Periera

  • 1Department of Physiology, University of Wisconsin Medical School, Madison, WI, USA. rimoss@physiology.wisc.edu

Circulation Research
|April 14, 2000
PubMed
Summary

No abstract available in PubMed .

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