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Updated: Apr 18, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Left ventricular noncompaction cardiomyopathy: adult association with 1p36 deletion syndrome
James Lee1, Sarah Rinehart1, Venkateshewar Polsani1
1Piedmont Heart Institute, Atlanta, Georgia.
No abstract available in PubMed .
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