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Updated: Oct 30, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
A Novel Variant of COL6A2 Gene Causing Bethlem Myopathy and Evaluation of Essential Hypertension
M Gultekin Kutluk1, Naz Kadem2, Omer Bektas3
1Department of Paediatric Neurology, Antalya Research and Training Hospital, Antalya, Turkey.
No abstract available in PubMed .
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