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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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ACTA1 Novel Likely Pathogenic Variant in a Family With Dilated Cardiomyopathy
Nosheen Reza1, Ankit Garg2, Shana L Merrill1
1Division of Cardiovascular Medicine, Department of Medicine, Center for Inherited Cardiovascular Disease (N.R., S.L.M., J.L.C., A.T.O.), Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Circulation. Genomic and Precision Medicine
|October 26, 2018
Abstract
No abstract available in PubMed .
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