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Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy.
Protein & Cell ( IF 21.1 ) Pub Date : 2021-04-22 , DOI: 10.1007/s13238-021-00843-w Bin Li 1, 2 , Yongkun Zhan 1 , Qianqian Liang 1, 3 , Chen Xu 1, 3 , Xinyan Zhou 1 , Huanhuan Cai 1 , Yufan Zheng 1 , Yifan Guo 1 , Lei Wang 4 , Wenqing Qiu 4 , Baiping Cui 1 , Chao Lu 1, 3 , Ruizhe Qian 1, 3 , Ping Zhou 1 , Haiyan Chen 5 , Yun Liu 4 , Sifeng Chen 1 , Xiaobo Li 1 , Ning Sun 1, 3, 6
中文翻译：
等基因人类多能干细胞疾病模型显示，ABRA缺乏症是cTnT突变诱导的家族性扩张型心肌病的基础。
更新日期：2021-04-22
Protein & Cell ( IF 21.1 ) Pub Date : 2021-04-22 , DOI: 10.1007/s13238-021-00843-w Bin Li 1, 2 , Yongkun Zhan 1 , Qianqian Liang 1, 3 , Chen Xu 1, 3 , Xinyan Zhou 1 , Huanhuan Cai 1 , Yufan Zheng 1 , Yifan Guo 1 , Lei Wang 4 , Wenqing Qiu 4 , Baiping Cui 1 , Chao Lu 1, 3 , Ruizhe Qian 1, 3 , Ping Zhou 1 , Haiyan Chen 5 , Yun Liu 4 , Sifeng Chen 1 , Xiaobo Li 1 , Ning Sun 1, 3, 6
Affiliation
中文翻译：
等基因人类多能干细胞疾病模型显示，ABRA缺乏症是cTnT突变诱导的家族性扩张型心肌病的基础。
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