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Updated: Aug 16, 2026

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Gene symbol: ATP7B. Disease: Wilson disease
1Human Genetics and Genomics Division, Indian Institute of Chemical Biology, 4 Raja S.C. Mullick Road, Kolkata-700 032, West Bengal, India. thisiskr@rediffmail.com
Human Genetics
|September 13, 2005
Abstract
No abstract available in PubMed .
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