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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Sarcomere lego to understand myofilament dysfunction underlying hypertrophic cardiomyopathy due to gene mutations
1Department of Cardiac Physiology, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan.
The Journal of Physiology
|September 19, 2025
Abstract
No abstract available in PubMed .
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