Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy
同源人类多能干细胞疾病模型揭示ABRA缺陷是cTnT突变诱发的家族性扩张型心肌病的基础。
期刊:Protein & Cell
影响因子:12.8
doi:10.1007/s13238-021-00843-w
Li, Bin; Zhan, Yongkun; Liang, Qianqian; Xu, Chen; Zhou, Xinyan; Cai, Huanhuan; Zheng, Yufan; Guo, Yifan; Wang, Lei; Qiu, Wenqing; Cui, Baiping; Lu, Chao; Qian, Ruizhe; Zhou, Ping; Chen, Haiyan; Liu, Yun; Chen, Sifeng; Li, Xiaobo; Sun, Ning
