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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
1University of Palermo, Palermo, Italy. salvatore.novo@unipa.it
Cardiomyopathies (CM) are complex myocardial diseases, often genetic, posing diagnostic challenges. Echocardiography is a key tool for identifying CM clinical features and aiding physician assessment.
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