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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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A novel RHD allele caused by c.767 C>T mutation was identified in a Chinese individual

Hongjuan Lyu1, Kun Wang1, Zhihui Feng2

  • 1Obstetrics Department, Qingdao Women and Children's Hospital, Qingdao, P. R. China.

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|April 2, 2024
PubMed
Abstract

No abstract available in PubMed .

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