Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long-QT syndrome

Author(s):
Bellin, M.; Casini, S.; Davis, R.P. (0000-0002-7917-9423); D'Aniello, C.; Haas, J.; Ward-van Oostwaard, D.; Tertoolen, L.G.J.; Jung, C.B.; Elliott, D.A.; Welling, A.; Laugwitz, K.L.; Moretti, A.; Mummery, C.L. (0000-0002-4549-6535)
Published
2013
Publication type
Article / Letter to editor
gene targetingHERGhuman embryonic stem cellsinduced pluripotent stem cellslong-QT syndrome
Date issued
2013-12-11
Language
English
Is part of
EMBO Journal (2013), Vol. 32, no. 24, p. 3161-3175
hdl
1887/101811
doi
10.1038/emboj.2013.240