Related Experiment Video

Updated: Jun 1, 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

Cardiomyopathy with alopecia and palmoplantar keratoderma (CAPK) is caused by a JUP mutation

H Erken1, K O Yariz, D Duman

  • 1Departments of Cardiology Pathology, Ankara University School of Medicine, Sihhiye, Ankara 06100, Turkey.

The British Journal of Dermatology
|June 15, 2011
PubMed

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