KLF13 Loss‐of‐Function Mutations Underlying Familial Dilated Cardiomyopathy

KLF13 Loss‐of‐Function Mutations Underlying Familial Dilated Cardiomyopathy

Background Dilated cardiomyopathy (DCM), characterized by progressive left ventricular enlargement and systolic dysfunction, is the most common type of cardiomyopathy and a leading cause of heart failure and cardiac death. Accumulating evidence underscores the critical role of genetic defects in the...

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Bibliographic Details
Main Authors: Yu‐Han Guo, Jun Wang, Xiao‐Juan Guo, Ri‐Feng Gao, Chen‐Xi Yang, Li Li, Yu‐Min Sun, Xing‐Biao Qiu, Ying‐Jia Xu, Yi‐Qing Yang
Format: Article
Language:English
Published: Wiley 2022-11-01
Series:Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Subjects:
biological assay
dilated cardiomyopathy
functional genomics
KLF13
molecular genetics
transcriptional factor
Online Access:https://www.ahajournals.org/doi/10.1161/JAHA.122.027578

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https://www.ahajournals.org/doi/10.1161/JAHA.122.027578

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