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Updated: Mar 17, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
The L-type Ca2+ channel: A mediator of hypertrophic cardiomyopathy
Helena M Viola1, Livia C Hool1,2
1a School of Anatomy, Physiology and Human Biology, The University of Western Australia , Crawley , WA , Australia.
No abstract available in PubMed .
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