Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: Evidence for clinically significant IKr-IKs α-subunit interaction
Keywords: LQTS، سندرم طولانی QT; Long QT syndrome; KCNQ1; KCNH2; Torsades de pointes; Sudden cardiac deathAU, arbitrary units; CHO, Chinese hamster ovary; dn, dominant negative; ER, endoplasmic reticulum; E1, KCNE1; HEK, human embryonic kidney; H2, KCNH2; LQTS, long QT syndrome; OD, opti