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Mutated KCNH2 activates type II hereditary long QT syndrome. 1 / 1

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"Mutations of the HERG gene can cause type II hereditary long QT syndrome (LQT2), characterized by prolongation of the QT interval, abnormal T wave, torsade de pointes, syncope and sudden cardiac death."

26829745

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Mutated KCNH2 activates type II hereditary long QT syndrome. 1 / 1

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