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


Bellin M, Casini S, Davis RP, D'Aniello C, Haas J, Ward-van Oostwaard D, Tertoolen LG, Jung CB, Elliott DA, Welling A, Laugwitz KL, Moretti A, Mummery CL

EMBO J. 2013, 32(24), 3161-75