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KCNQ1 activates LQT syndrome type 1. 2 / 2

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"LQT syndrome type 1 (LQT1) is caused by a mutation in KCNQ1 (also known as KVLQT1 or K v7.1), which encodes the pore forming alpha subunits of the channels that generate I Ks, an adrenergic sensitive slow outward potassium current."

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"LQT syndrome type 1 (LQT1) is caused by a mutation in the KCNQ1 gene, leading to abnormalities in encoding the channels that regulate potassium current [XREF_BIBR]."

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KCNQ1 activates LQT syndrome type 1. 2 / 2

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