Related Experiment Video
Updated: May 30, 2025

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
3.0K
Mono and Biallelic Variants in TRIM63 Are Frequently Associated With a Unique Form of Hypertrophic Cardiomyopathy
Noa Ruhrman Shahar1, Dina Marek-Yagel2, Rotem Greenberg3
1Raphael Recanati Genetic Institute (N.R.S., O.I., E.F., L. Bazak, L.B.S.), Rabin Medical Center, Petach Tikva, Israel.
Circulation. Genomic and Precision Medicine
|January 27, 2025
Abstract
No abstract available in PubMed .
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