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Paper Details

Physiological genomics identifies genetic modifiers of long QT syndrome type 2 severity.
J Clin Invest
43
2018
Ca2+, Congenital long QT syndrome, GTP, GTP-binding protein REM2, KCNH2, KCNK17, LQT2, LQTS, LQTS type 2, R752W, REM2, REM2 variant, arrhythmias, hERG, hERG R752W mutation, iPSC-CMs, induced pluripotent stem cell-derived cardiomyocytes, inherited channelopathy, long QT syndrome type 2, modifier genes, monogenic disorder, patients, potassium
Author NameAffiliation
Paul J TesarCase Western Reserve University
Elizabeth S KaufmanHeart and Vascular Research Center
Alfred L GeorgeNorthwestern University
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Datasets

Release 1.2