Related Experiment Video

Updated: Aug 23, 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

[Behcet disease: uncommon cause of myocardial infarction]

S Kraiem1, S Fennira, K Battikh

  • 1Service de cardiologie, hôpital Habib-Thameur, 8, rue Ali-Ben-Ayed, Montfleury 1008 Tunis, Tunisie. mailto.mejri@etap.com.tn

Annales De Cardiologie Et D'Angeiologie
|June 30, 2004
PubMed

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