Spectrum of Mutations in Long-QT Syndrome Genes : KVLQT1, HERG, SCN5A, KCNE1, and KCNE2. Circulation 2000 102 : 1178 –85. [3] Neyroud N, Tesson F, Denjoy I, et al.
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A novel mutation in the K + channel KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome.
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