Analysis of the human KCNH2(HERG) gene:
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Aimée Paulussen; Ping Yang; Menelas Pangalos; Peter Verhasselt; Roger Marrannes;
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Article
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2000
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John Wiley and Sons
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English
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Long QT (LQT) syndrome is a potentially life-threatening disorder, characterized by a distinct cardiac arrhythmia known as torsades de pointes. Mutations within a number of genes linked to the familial form, including that coding for a cardiac potassium channel called KCNH2 (HERG), have been describ