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Updated: May 22, 2025

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
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Family history of aortic dissection in fibrillin-1 pathogenic variant
Maria Tchitchinadze1, Olivier Milleron1, Ludivine Eliahou1
1Centre National de Reference Pour le Syndrome de Marfan et Apparentés, VASCERN HCP, Service de Cardiologie, AP-HP, Hôpital Bichat, 46 rue Henri Huchard, Paris 75018, France.
European Heart Journal
|May 21, 2025
Abstract
No abstract available in PubMed .
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