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Updated: Nov 30, 2025

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
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Patients With Hypertrophic Cardiomyopathy Deemed Genotype Negative Based on Research Grade Genetic Analysis: Time for
Bailey J O'Hare1, J Martijn Bos1, David J Tester1
1Department of Molecular Pharmacology and Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, MN (B.J.O., J.M.B., D.J.T., M.J.A.).
Circulation. Genomic and Precision Medicine
|November 16, 2020
Abstract
No abstract available in PubMed .
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