IndraLab

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KCNQ1 activates LQT-1. 1 / 1
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"Genetic mutations in the alpha- (KCNQ1) and beta- (KCNE1) subunits of I (Ks) underlie Long QT Syndrome type 1 and 5 (LQT-1 and LQT-5), respectively, and predispose carriers to the development of polymorphic ventricular arrhythmias and sudden cardiac death."