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Updated: Mar 7, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Novel Dominant-Negative Mutation in Cardiac Troponin I Causes Severe Restrictive Cardiomyopathy
Saumya Shah1, Haran Yogasundaram1, Ratnadeep Basu1
1From the Division of Cardiology, Department of Medicine (S.S., H.Y., R.B., F.W., D.I.P., G.Y.O.) and Mazankowski Alberta Heart Institute (S.S., H.Y., R.B., D.I.P., G.Y.O.), University of Alberta, Edmonton, Canada; and Blueprint Genetics Inc, San Francisco, CA (T.-P.A.).
No abstract available in PubMed .
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