Related Experiment Video
Updated: Jan 22, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
X-linked hypohidrotic ectodermal dysplasia: clinical and molecular genetic analysis of a large Russian family with a
T B Milovidova1, O A Schagina1, M V Freire1
1Federal State Budgetary Scientific Institution "Research Centre for Medical Genetics", Moscow, Russia.
No abstract available in PubMed .
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