KCNE1 mutations cause Jervell and Lange-Nielsen syndrome
Authors:
- Eric Schulze-BahrESEric Schulze-Bahr
- Qing WangQWQing Wang
- Horst WedekindHWHorst Wedekind
- Wilhelm HaverkampWHWilhelm Haverkamp
- Qiuyun ChenQCQiuyun Chen
- Yaling SunYSYaling Sun
- Claudia RubleCRClaudia Ruble
- Marco HördtMHMarco Hördt
- Jeffrey A. TowbinJTJeffrey A. Towbin
- Martin BorggrefeMBMartin Borggrefe
- Gerd AssmannGAGerd Assmann
- Xiangdong QuXQXiangdong Qu
- 1 November 1997
- journal article
- Published by Springer Nature in Nature Genetics
- Vol. 17 (3) , 267-268
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Molecular Basis of the Long-QT Syndrome Associated with DeafnessNew England Journal of Medicine, 1997
- A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndromeNature Genetics, 1997
- Coassembly of KVLQT1 and minK (IsK) proteins to form cardiac IKS potassium channelNature, 1996
- KvLQT1 and IsK (minK) proteins associate to form the IKS cardiac potassium currentNature, 1996
- Exclusion of KCNE1 (IsK) as a Candidate Gene for Jervell and Lange-Nielsen SyndromeJournal of Molecular and Cellular Cardiology, 1996
- Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmiasNature Genetics, 1996
- The Long-QT SyndromeNew England Journal of Medicine, 1995
- Polymorphism of the gene encoding a human minimal potassium ion channel (minK)Gene, 1994
- Cellular localization of rat Isk protein in the stria vascularis by immunohistochemical observationHearing Research, 1991
- Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden deathAmerican Heart Journal, 1957