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Updated: Jun 16, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
[Ehlers-Danlos syndrome type I: importance of genetic diagnosis]
C Lobete Prieto1, I Llano Rivas, J Fernández Toral
1Unidad de Genética, Hospital Universitario Central de Asturias, Oviedo, España. carloslobete@hotmail.com <carloslobete@hotmail.com>
No abstract available in PubMed .
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