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Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes

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Year: 2009
Type: article
Source: Journal of Molecular and Cellular Cardiology
DOI: 10.1016/j.yjmcc.2009.10.011
Authors: Thomas Z. Armel, Leslie A. Leinwand
Institution: University of Colorado Boulder
Language: English

Topic: Cardiomyopathy and Myosin Studies
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: green

Funders: National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences
Awards: Interdisciplinary Predoctoral Training in Molecular Biophysics, Mechanisms of myopathy caused by mutations in the myosin rod
OpenAlex ID: W2039411908
FWCI: 3.02
Cites: 25
Cited by: 33
Related to: 10
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