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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Anjali A Wagle1, Ria Gupta1, Maham Karatela1
1Division of Cardiology, Department of Medicine, The Johns Hopkins University, Baltimore, Maryland, USA.
Genetic cardiomyopathies and cardiac sarcoidosis can be difficult to distinguish. This study highlights that cardiac imaging is not always specific in patients with known genetic heart conditions, requiring individualized patient assessment.
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