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Updated: Oct 13, 2025

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
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CACNA1S mutation associated with a case of juvenile-onset congenital myopathy
Eleonora Mauri1, Daniela Piga1, Serena Pagliarani2
1IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy.
Journal of the Neurological Sciences
|November 11, 2021
Abstract
No abstract available in PubMed .
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