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KCNH2 activates long QT syndrome type 2. 3 / 3

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"Mutations in hERG cause the congenital form of long QT syndrome type 2 (LQT2), an inherited autosomal dominant disorder characterized by prolonged QT interval on the electrocardiogram."

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"The long QT syndrome type 2 (LQT2) is caused by mutations in the human ether-a-go-go-related gene (hERG, KCNH2)."

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"Dysfunction of the HERG channel can cause long QT syndrome type 2 (LQT2)."

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KCNH2 activates long QT syndrome type 2. 3 / 3

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