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KCNH2 activates type 2 long QT syndrome. 1 / 1

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"Mutations in the KCNH2 gene were reported to cause type 2 long QT syndrome (LQT2), a rare inherited ion channel disorder characterized by prolonged QT interval and predisposing patients to ventricular arrhythmias that can lead to syncope and sudden cardiac death (SCD)."

27064559

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KCNH2 activates type 2 long QT syndrome. 1 / 1

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