Related Experiment Video
Updated: Jul 10, 2026

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Sarcomere dysfunction as the molecular basis of hypertrophic cardiomyopathy
Saif F Dababneh1, Thomas M Roston2,3
1MD/PhD Program, Faculty of Medicine, The University of British Columbia, Vancouver, British Columbia, Canada. saifdab@student.ubc.ca.
Nature Reviews. Cardiology
|July 8, 2026
Abstract
No abstract available in PubMed .
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