IndraLab

Statements


KCNQ1 inhibits Type 1 long QT syndrome. 2 / 2
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"Type 1 long QT syndrome (LQT1) is caused by loss-of-function mutations in the KCNQ1 encoded Kv7.1 channel that conducts the slowly activating component of the delayed rectifier K + current (I Ks)."

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"Type 1 long QT syndrome (LQT1) accounts for ~ 35% of LQTS and is caused by loss-of-function mutations in the KCNQ1 K + channel (Kv7.1)."