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Updated: Feb 19, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
The missing link in heart failure: a case of cobalt cardiomyopathy uncovered through medical history
Jesús Rivera-Del-Amo1, Paula Bolea-Ramos1, William Delgado-Nava1
1Cardiology Department.
No abstract available in PubMed .
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