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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 mutations in B3GALNT2 gene causing α-dystroglycanopathy in Chinese patients
Xiao-Yu Chen1, Dan-Yu Song1, Yan-Bin Fan1
1Department of Pediatrics, Peking University First Hospital, Beijing 100034, China.
Chinese Medical Journal
|December 8, 2020
Abstract
No abstract available in PubMed .
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