Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleIsogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy.AuthorsLi, 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, NingPublicationProtein & Cell, 2022, Vol 13, Issue 1, p65ISSN1674-800XPublication typeLetterDOI10.1007/s13238-021-00843-w