Potassium Channelopathies
- 1 June 1997
- journal article
- review article
- Published by Elsevier in Neuropharmacology
- Vol. 36 (6) , 755-762
- https://doi.org/10.1016/s0028-3908(97)00029-4
Abstract
No abstract availableKeywords
This publication has 48 references indexed in Scilit:
- KvLQT1 and IsK (minK) proteins associate to form the IKS cardiac potassium currentNature, 1996
- Genetically Defined Therapy of Inherited Long-QT SyndromeCirculation, 1996
- K+ channels: generating excitement in pancreatic beta-cellsDiabetes, 1996
- Missense Mutation in the Pore Region of HERG Causes Familial Long QT SyndromeCirculation, 1996
- Episodic ataxia results from voltage-dependent potassium channels with altered functionsNeuron, 1995
- Identification of two new KCNA1 mutations in episodic ataxia/myokymia familiesHuman Molecular Genetics, 1995
- Heterologous Multimeric Assembly Is Essential for K+ Channel Activity of Neuronal and Cardiac G-Protein-Activated Inward RectifiersBiochemical and Biophysical Research Communications, 1995
- A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndromeCell, 1995
- Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1Nature Genetics, 1994
- Familial periodic cerebellar ataxia: A problem of cerebellar intracellular pH homeostasisAnnals of Neurology, 1992