Related Experiment Video
Updated: Jul 8, 2026

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Camisa disease: a rare variant of Vohwinkel's syndrome
Indian Journal of Dermatology, Venereology and Leprology
|January 15, 2008
Abstract
No abstract available in PubMed .
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