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Updated: Feb 17, 2026

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

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A Familial Thoracic Aortic and Arterial Aneurysm Syndrome Associated With FBN2 (Y1311C) and MYH11 (R34T) Variants: A

Akhtar Purvez1,2, Ana Mir3, Mudhasir Bashir4

  • 1Clinical Research, Momentum Medical Research, Charlottesville, USA.

Cureus
|February 16, 2026
PubMed

Keywords:
aortic root dilationfamilial aortopathyfbn2 mutationheritable thoracic aortic diseasemyh11 mutation

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