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

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

doi:10.1007/s13238-021-00843-w

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Protein Cell ›› 2022, Vol. 13 ›› Issue (1) : 65-71. DOI: 10.1007/s13238-021-00843-w

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

Bin Li¹^,² ,
Yongkun Zhan¹ ,
Qianqian Liang¹^,⁴ ,
Chen Xu¹^,⁴ ,
Xinyan Zhou¹ ,
Huanhuan Cai¹ ,
Yufan Zheng¹ ,
Yifan Guo¹ ,
Lei Wang⁶ ,
Wenqing Qiu⁶ ,
Baiping Cui¹ ,
Chao Lu¹^,⁴ ,
Ruizhe Qian¹^,⁴ ,
Ping Zhou¹ ,
Haiyan Chen⁵ ,
Yun Liu⁶ ,
Sifeng Chen¹ ,
Xiaobo Li¹ ,
Ning Sun¹^,³^,⁴

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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. Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy. Protein Cell, 2022, 13(1): 65‒71 https://doi.org/10.1007/s13238-021-00843-w

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