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Updated: May 16, 2025

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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
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Novel Compound Heterozygous Mutation on MYORG Gene in a Chinese Patient with Primary Familial Brain Calcification
Jixiang Lin1, Yanfei Wang2, Xiang Gao3
1Department of Neurology, Shandong Provincial Qianfoshan Hospital, Shandong University of Traditional Chinese Medicine, Jinan, Shandong Province, People's Republic of China.
Neurology India
|April 3, 2025
Abstract
No abstract available in PubMed .
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