IndraLab

Statements


KCNQ1 activates sqt-3. 2 / 2
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"Specifically, the SQT1, SQT2, and SQT3 subtypes are caused by gain-of-function mutations in the KCNH2, KCNQ1, and KCNJ2 genes, respectively."

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"SQTS has been associated with the gain-of-function mutations in 3 distinct potassium channels, KCNH2, KCNQ1 and KCNJ2, which cause SQT1, SQT2 and SQT3, respectively [111-114]."