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Updated: Aug 26, 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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A novel MAP3K20 mutation causing centronuclear myopathy-6 with fiber-type disproportion in a Pakistani family
Ilyas Ahmad1,2,3,4, Ayaz Khan5, Hafiza Noor Ul Ayan6,5
1Institute for Cardiogenetics, University of Lübeck, Lübeck, Germany. ilyas.ahmad@uni-luebeck.de.
Journal of Human Genetics
|October 10, 2022
Abstract
No abstract available in PubMed .
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