IndraLab

Statements

KCNQ1 activates LQT2. 4 / 4
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"LQT1, LQT2, and LQT3 are caused by mutations in KCNQ1 (LQT1), KCNH2 (LQT2), and SCN5A (LQT3), which account for approximately 90% of genotyped LQTS patients."
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"[XREF_BIBR] A total of 16 genes associate with LQTS, and mutations in KCNQ1 or KCNH2 genes cause the most common subtypes LQT1 and LQT2, respectively."
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"LQT1 and LQT2 are caused by gene mutations in KCNQ1 and KCNH2, respectively, and mutations in these 2 genes are responsible for about 85% of LQTS linked mutations."
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"Among them most common are LQT1, LQT2, and LQT3, caused by mutations in KCNQ1, KCNH2, and SCN5A genes, respectively (Splawski etal."
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