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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Haber's syndrome: report of two Chinese families
Zai-Ming Chen1, Li-Ming Wu2, Ferina Ismail3
1Department of Dermatology, Taizhou Second People's Hospital, Zhejiang, China.
International Journal of Dermatology
|February 26, 2022
Abstract
No abstract available in PubMed .
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