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KCNH2 activates type 2 long QT (LQT2) [. 1 / 1

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"Among some 200 hereditary mutations in KCNH2 that cause type 2 long QT (LQT2) [XREF_BIBR], about 67% are missense alterations, the majority of which cause trafficking defects; that is, an overall reduction of cell surface hERG protein [XREF_BIBR]."

18096051

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IndraLab

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KCNH2 activates type 2 long QT (LQT2) [. 1 / 1

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