Frameshift variants in C10orf71 cause dilated cardiomyopathy in human, mouse, and organoid models.

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作者： Yang,Li ^[1] ; Ke,Ma ^[2] ; Zhujun,Dong ^[3] ; Shijuan,Gao ^[1] ; Jing,Zhang ^[2] ; Shan,Huang ^[3] ; Jie,Yang ^[1] ; Guangming,Fang ^[2] ; Yujie,Li ^[3] ; Xiaowei,Li ^[1] ; Carrie,Welch ^[2] ; Emily L,Griffin ^[3] ; Prema,Ramaswamy ^[1] ; Zaheer,Valivullah ^[2] ; Xiuying,Liu ^[3] ; Jianzeng,Dong ^[1] ; Dao Wen,Wang ^[2] ; Jie,Du ^[3] ; Wendy K,Chung ^[1] ; Yulin,Li ^[2]

作者单位： Beijing Anzhen Hospital, Capital Medical University, Beijing, China. ^[1] Beijing Institute of Heart, Lung & Blood Vessel Disease, Beijing, China. ^[2] The Key Laboratory of Remodeling-Related Cardiovascular Diseases, Ministry of Education, Beijing, China. ^[3] Novogene Co. Ltd., Beijing, China. ^[4] Department of Cardiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China. ^[5] Department of Pediatrics, Columbia University, New York, New York, USA. ^[6] Maimonides Medical Center, New York, New York, USA. ^[7] Broad Institute, Cambridge, Massachusetts, USA. ^[8] Changping Laboratory, Beijing, China. ^[9] Division of Cardiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. ^[10] Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA. ^[11]

关键词 Cardiology Cardiovascular disease Genetic diseases Genetic variation Genetics