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Mutated KCNH2 inhibits long QT syndrome type 2. 1 / 1

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"Functional impairment of the hERG channel can result in inherited and acquired long QT syndrome type 2 (LQT2), caused by mutations of the hERG or off-target effects of diverse therapeutic agents, respectively [XREF_BIBR]."

28763460

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IndraLab

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Mutated KCNH2 inhibits long QT syndrome type 2. 1 / 1

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