Generation of eight human induced pluripotent stem cell (iPSC) lines from familial Long QT Syndrome type 1 (LQT1) patients carrying KCNQ1 c.1697C>A mutation (NUIGi005-A, NUIGi005-B, NUIGi005-C, NUIGi006-A, NUIGi006-B, NUIGi006-C, NUIGi007-A, and NUIGi007-B)

Long QT Syndrome type 1 (LQT1), an inherited cardiac ion channelopathy associated with arrhythmias and risk of sudden death, is caused by mutations in KCNQ1 encoding the α-subunit of Kv7.1, that affects the slow component of delayed rectifier K+ current (IKs) channel. In this study, the non-integrat...

Popoln opis

Bibliografske podrobnosti

Principais autores:	Ning Ge, Min Liu, Janusz Krawczyk, Veronica McInerney, Joseph Galvin, Sanbing Shen, Timothy O'Brien, Terence Prendiville
Format:	Artigo
Jezik:	Inglês
Izdano:	Elsevier 2019-08-01
Serija:	Stem Cell Research
Online dostop:	http://www.sciencedirect.com/science/article/pii/S1873506119301321
Oznake:	Označite Brez oznak, prvi označite!