Characterization and Subcellular Localization of KCNQ1 with a Heterozygous Mutation in the C Terminus
- 1 February 2001
- journal article
- Published by Elsevier in Journal of Molecular and Cellular Cardiology
- Vol. 33 (2) , 197-207
- https://doi.org/10.1006/jmcc.2000.1300
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden deathPublished by Elsevier ,2004
- The Dominant Negative LQT2 Mutation A561V Reduces Wild-type HERG ExpressionPublished by Elsevier ,2000
- N‐linked glycosylation sites determine HERG channel surface membrane expressionThe Journal of Physiology, 1999
- A Dominant Negative Isoform of the Long QT Syndrome 1 Gene ProductPublished by Elsevier ,1998
- 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
- SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndromeCell, 1995
- A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndromeCell, 1995
- CONGENITAL CARDIAC ARRHYTHMIAThe Lancet, 1965