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

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Higher Education Press 2021
Materias:
Letter
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8776971/
https://www.ncbi.nlm.nih.gov/pubmed/33884582
http://dx.doi.org/10.1007/s13238-021-00843-w
Descripción
Sumario:

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