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Updated: Sep 30, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
03:45

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

Published on: August 8, 2022

A rare variant of single coronary artery and non-obstructive hypertrophic cardiomyopathy

Yusuf Atmaca1, Rabih Dandachi, Dervis Oral

  • 1Ankara University, Faculty of Medicine, Department of Cardiology, Turkey. yusufatmaca1@yahoo.com

The Journal of Invasive Cardiology
|July 31, 2002
PubMed

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