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MYH7B variants cause hypertrophic cardiomyopathy by activating the CaMK-signaling pathway |
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| Authors: | Chen Peng Li Zongzhe Nie Jiali Wang Hong Yu Bo Wen Zheng Sun Yang Shi Xiaolu Jin Li Wang Dao-Wen |
| Institution: | 1.Division of Cardiology, Departments of Internal Medicine and Genetic Diagnosis Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China ;2.Hubei Key Laboratory of Genetics and Molecular Mechanism of Cardiological Disorders, Wuhan, 430030, China ;3.Collaborative Innovation Center for Genetics and Development, School of Life Sciences, Fudan University, Shanghai, 200438, China ;4.Experimental Research Center, China Academy of Chinese Medical Sciences, Beijing, 100700, China ; |
| Abstract: | Science China Life Sciences - Hypertrophic cardiomyopathy (HCM) is a common genetic disease, predominantly caused by mutations in cardiac sarcomere genes; however, whether MYH7B causes HCM is not... |
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