Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy. Issue 1 (22nd April 2021)

Record Type:: Journal Article
Title:: Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy. Issue 1 (22nd April 2021)
Main Title:: Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy
Authors:: 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
Abstract:
Is Part Of:: Protein & cell. Volume 13:Issue 1(2022)
Journal:: Protein & cell
Issue:: Volume 13:Issue 1(2022)
Issue Display:: Volume 13, Issue 1 (2022)
Year:: 2022
Volume:: 13
Issue:: 1
Issue Sort Value:: 2022-0013-0001-0000
Page Start:: 65
Page End:: 71
Publication Date:: 2021-04-22
Subjects:: Proteins -- Periodicals
Cells -- Periodicals
Cytology -- Periodicals
572.6
Journal URLs:: https://academic.oup.com/proteincell ↗
http://www.springer.com/gb/ ↗
DOI:: 10.1007/s13238-021-00843-w ↗
Languages:: English
ISSNs:: 1674-800X
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 6935.930000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 25742.xml