PubMed 9328483
Referenced in: none
Automatically associated channels: Kv2.1 , Kv7.1 , Slo1
Title: 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.
Authors: J Tyson, L Tranebjaerg, S Bellman, C Wren, J F Taylor, J Bathen, B Aslaksen, S J Sørland, O Lund, S Malcolm, M Pembrey, S Bhattacharya, M Bitner-Glindzicz
Journal, date & volume: Hum. Mol. Genet., 1997 Nov , 6, 2179-85
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/9328483
Abstract