Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy

Protein Cell. 2021 Apr 22. doi: 10.1007/s13238-021-00843-w. Online ahead of print.NO ABSTRACTPMID:33884582 | DOI:10.1007/s13238-021-00843-w

Source: Protein and Cell - April 22, 2021 Category: Cytology Authors: Bin Li Yongkun Zhan Qianqian Liang Chen Xu Xinyan Zhou Huanhuan Cai Yufan Zheng Yifan Guo Lei Wang Wenqing Qiu Baiping Cui Chao Lu Ruizhe Qian Ping Zhou Haiyan Chen Yun Liu Sifeng Chen Xiaobo Li Ning Sun Source Type: research