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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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LMNA Q353R Mutation Causes Dilated Cardiomyopathy Through Impaired Vitamin D Signaling
Masamichi Ito1,2, Manami Katoh1,3,4, Tatsuro Sassa1
1Department of Cardiovascular Medicine (M. Ito, M. Katoh, T.S., T.K., K.F., S.Y., M. Katagiri, M. Kubota, T.Y., S.H., H.M., S.N., I.K.), Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Japan.
Circulation
|September 16, 2024
Abstract
No abstract available in PubMed .
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