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Updated: May 24, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
[Heart involvement in sarcoglycanopathies]
A Fayssoil1, O Nardi, D Orlikowski
1Réanimation médicale, université Versailles SQY, CHU Raymond-Poincaré, 104 boulevard Raymond-Poincaré, Garches, France. Fayssoil2000@yahoo.fr
Abstract:
Sarcoglycanopathies (SG) are autosomic recessive muscular dystrophies, secondary to mutations of the sarcoglycan complex. Clinical pictures include muscle weakness affecting mainly the proximal limb girdle musculature. We review heart involvement in this group of disease.
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