Modulating Beta-Cardiac Myosin Function at the Molecular and Tissue Levels
Inherited cardiomyopathies are a common form of heart disease that are caused by mutations in sarcomeric proteins with beta cardiac myosin ( ) being one of the most frequently affected genes. Since the discovery of the first cardiomyopathy associated mutation in beta-cardiac myosin, a major goal has...
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Veröffentlicht in: | Frontiers in physiology 2017-01, Vol.7, p.659-659 |
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