Therapeutic potential of AAV9-S15D-RLC gene delivery in humanized MYL2 mouse model of HCM
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DOI: 10.1007/s00109-019-01791-z
Abstract: Familial hypertrophic cardiomyopathy (HCM) is an autosomal dominant disorder characterized by ventricular hypertrophy, myofibrillar disarray, and fibrosis, and is primarily caused by mutations in sarcomeric genes. With no definitive cure for HCM, there is an… read more here.
Keywords: rlc; hcm; s15d rlc; gene ... See more keywords