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Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Higher Education Press
2021
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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 |
description | |
format | Online Article Text |
id | pubmed-8776971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Higher Education Press |
record_format | MEDLINE/PubMed |
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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