| 1 | JLNS2, JLNS1, KCNQ1
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| Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen.
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| Tyson J, Tranebjaerg L, McEntagart M, Larsen LA, Christiansen M, Whiteford ML, Bathen J, Aslaksen B, Sorland SJ, Lund O, Pembrey ME, Malcolm S, Bitner-Glindzicz M.
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| Hum Genet 107(5):499-503. Erratum in: Hum Genet 2001 Jan;108(1):75. 2000
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| 2 | JLNS2, KCNE1, KCNF1, KCNQ1
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| Genomic structure of three long QT syndrome genes : KVLQT1, HERG, and KCNE1.
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| Splawski I, et al.
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| Genomics 51 : 86-97. 1998
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| 3 | JLNS1, JLNS2, KCNQ1, KCNE1
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| IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome.
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| Tyson J, Tranebjaerg L, Bellman S, Wren C, Taylor JF, Bathen J, Aslaksen B, Sorland SJ, Lund O, Malcolm S, Pembrey M, Bhattacharya S, Bitner-Glindzicz M.
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| Hum Mol Genet 6(12):2179-85. 1997
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| 4 | JLNS2, KCNE1
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| KCNE1 mutations cause Jervell and Lange-Nielsen syndrome.
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| Schulze-Bahr E, Wang Q, Wedekind H, Haverkamp W, Chen Q, Sun Y, Rubie C, Hordt M, Towbin JA, Borggrefe M, Assmann G, Qu X, Somberg JC, Breithardt G, Oberti C, Funke H.
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| Nat Genet 17(3):267-8. No abstract available. 1997
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