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Updated: Aug 10, 2026

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Molecular insights into the pathogenesis of hereditary haemochromatosis
1Centre for Haemochromatosis and Hereditary Liver Diseases, Department of Internal Medicine, University of Modena and Reggio Emilia, Policlinico, Via del Pozzo 71, 41100 Modena Italy. pietrangelo.antonello@unimore.it
Gut
|March 15, 2006
Abstract
No abstract available in PubMed .
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