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Updated: Dec 25, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
HYPERTROPHIC CARDIOMYOPATHY IN PATIENTS WITH 46 XX OR XY TURNER PHENOTYPE
Robert D. Leachman1, Roger A. Hurwitz, Roberto Lufschanowski
1Department of Cardiology, St. Luke's Episcopal Hospital, Houston, Texas.
No abstract available in PubMed .
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