Abstract 13599: A Truncated Mutation in Filamin C Reveals Non-myocyte Contributions to Hypertrophic Cardiomyopathy in Ipsc-derived Cardiac Fibroblasts
Circulation(2020)
Abstract
Introduction: Hypertrophic cardiomyopathy (HCM) is a cardiac genetic disorder that affects 1:500 individuals and represents one of the main causes of sudden cardiac death in young adults. Several m...
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Key words
hypertrophic cardiomyopathy,cardiac,non-myocyte,ipsc-derived
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