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Mutated KCNH2 inhibits LQT2. 1 / 1

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"Loss-of-function hERG mutations are well established to underlie the LQT2 form of congenital Long QT syndrome and, within the last decade, gain-of-function hERG mutations have been linked to the SQT1 form of the short QT syndrome."

24400172

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IndraLab

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Mutated KCNH2 inhibits LQT2. 1 / 1

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