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KCNH2-N588K inhibits SQT1. 1 / 1

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"The attenuated inactivation N588K HERG mutant used in this study has been shown recently to underlie the SQT1 familial form of the recently identified genetic ' Short QT syndrome ', which carries a risk of cardiac arrhythmia and sudden death XREF_BIBR."

17560554

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IndraLab

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KCNH2-N588K inhibits SQT1. 1 / 1

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