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Updated: Jul 20, 2025

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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Acanthosis Nigricans and Hypochondroplasia Associated with FGFR3 Mutation: A Case Report
Diego Soto-García1,2, Ana Batalla1,2, Marcos Oro-Ayude1,2
1From the Department of Dermatology, DIPO Research Group, Galicia Sur Health Research Institute (IIS Galicia Sur), SERGAS-UVIGO, Pontevedra, Spain.
Indian Journal of Dermatology
|August 2, 2023
Abstract
No abstract available in PubMed .
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