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Mutated KCNQ1 activates Long QT Syndrome (LQTS) Type 1. 1 / 1

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"KCNQ1 mutations underlie Long QT Syndrome (LQTS) Type 1 (LQT1), sub-classified as Romano Ward Syndrome (RWS; autosomal dominant) and Jervell Lange-Nielsen Syndrome (JLNS; typically autosomal recessive)."

20688187

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IndraLab

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Mutated KCNQ1 activates Long QT Syndrome (LQTS) Type 1. 1 / 1

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