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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.
Tyson J, Tranebjaerg L, Bellman S, Wren C, Taylor JF, Bathen J, Aslaksen B, Sørland SJ, Lund O, Malcolm S, Pembrey M, Bhattacharya S, Bitner-Glindzicz M. Tyson J, et al. Among authors: sorland sj. Hum Mol Genet. 1997 Nov;6(12):2179-85. doi: 10.1093/hmg/6.12.2179. Hum Mol Genet. 1997. PMID: 9328483
Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen.
Tyson J, Tranebjaerg L, McEntagart M, Larsen LA, Christiansen M, Whiteford ML, Bathen J, Aslaksen B, Sørland SJ, Lund O, Pembrey ME, Malcolm S, Bitner-Glindzicz M. Tyson J, et al. Among authors: sorland sj. Hum Genet. 2000 Nov;107(5):499-503. doi: 10.1007/s004390000402. Hum Genet. 2000. PMID: 11140949
Outcome of congenital heart defects--a population-based study.
Meberg A, Otterstad JE, Frøland G, Lindberg H, Sørland SJ. Meberg A, et al. Among authors: sorland sj. Acta Paediatr. 2000 Nov;89(11):1344-51. doi: 10.1080/080352500300002552. Acta Paediatr. 2000. PMID: 11106048
[Magnetic tomography in congenital heart defects].
Smevik B, Smith HJ, Bø G, Sørland SJ, Tjønneland S. Smevik B, et al. Among authors: sorland sj. Tidsskr Nor Laegeforen. 1990 Nov 30;110(29):3734-6. Tidsskr Nor Laegeforen. 1990. PMID: 2274940 Norwegian.
33 results