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Updated: Mar 28, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Application of Genetic Testing in Hypertrophic Cardiomyopathy for Preclinical Disease Detection
Jodie Ingles1, Charlotte Burns1, Alexandra Barratt1
1From the Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Sydney NSW, Australia (J.I., C.B., C.S.); Central Clinical School, Sydney Medical School, University of Sydney, Sydney NSW, Australia (J.I., C.B., C.S.); School of Population Health, Sydney Medical School, University of Sydney, Sydney NSW, Australia (A.B.); and Department of Cardiology, Royal Prince Alfred Hospital, Sydney NSW, Australia (J.I., C.B., C.S.).
No abstract available in PubMed .
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