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SCN5A activates LQT2. 1 / 1

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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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IndraLab

Statements

SCN5A activates LQT2. 1 / 1

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