IndraLab

Statements

KCNQ1 activates SQT2. 4 / 4
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"SQTS types 1 and 2 (SQT1 and SQT2) are caused by gain-of-function mutations in KCNH2 (also known as HERG ) and KCNQ1 (also known as KVLQT1 ), which encode the α subunit of the I Kr and I Ks channel, r[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
21215473
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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]."
30027834
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"A gain-of-function mutation in the KCNH2 gene encoding I kr (the rapidly activating delayed rectifier K + current) is responsible for the SQT1 [24] and a gain-of-function mutation in the KCNQ1 gene un[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
17561108