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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Ki Tae Yoon1,2, Hongqun Liu1, Samuel S Lee3
1Liver Unit, University Calgary Cumming School of Medicine, 3330 Hospital Dr NW, Calgary, AB, T2N 4N1, Canada.
Cirrhotic cardiomyopathy, a heart dysfunction in cirrhosis patients, stems from inflammation and altered cardiomyocyte function. Current management strategies require further investigation for optimal patient outcomes.
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