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Updated: Mar 16, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Glycogen Storage Disease Because of a PRKAG2 Mutation Causing Severe Biventricular Hypertrophy and High-Grade
Haran Yogasundaram1, Ian D Paterson1, Michelle Graham1
1From the Division of Cardiology, Department of Medicine (H.Y., I.D.P., M.G., G.Y.O.), Mazankowski Alberta Heart Institute (H.Y., I.D.P., M.G., G.Y.O.), and Department of Laboratory Medicine and Pathology (C.S.), University of Alberta, Edmonton, Canada.
No abstract available in PubMed .
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