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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:
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
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author 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
author_facet 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
author_sort Li, Bin
collection PubMed
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spelling pubmed-87769712022-02-02 Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy 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 Protein Cell Letter Higher Education Press 2021-04-22 2022-01 /pmc/articles/PMC8776971/ /pubmed/33884582 http://dx.doi.org/10.1007/s13238-021-00843-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Letter
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
Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy
title Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy
title_full Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy
title_fullStr Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy
title_full_unstemmed Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy
title_short Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy
title_sort isogenic human pluripotent stem cell disease models reveal abra deficiency underlies ctnt mutation-induced familial dilated cardiomyopathy
topic Letter
url 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
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