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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Carmen Ginghină1, Raluca Mihalache, B A Popescu
1Department of Cardiology, "Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania. carmenginghina2010@gmail.com
Restrictive cardiomyopathy (RCM) is rare and difficult to define, encompassing various heart conditions with distinct phenotypes. New classification systems focus on genotype-phenotype interactions for a better understanding of RCM.
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