Characterisation of the human voltage-gated potassium channel gene, KCNA7, a candidate gene for inherited cardiac disorders, and its exclusion as cause of progressive familial heart block I (PFHBI)
Open Access
- 1 January 2002
- journal article
- research article
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 10 (1) , 36-43
- https://doi.org/10.1038/sj.ejhg.5200739
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- A sodium-channel mutation causes isolated cardiac conduction diseaseNature, 2001
- Molecular biology of arrhythmic syndromesCurrent Opinion in Cardiology, 2000
- Cardiac conduction defects associate with mutations in SCN5ANature Genetics, 1999
- Genomic Organization, Chromosomal Localization, Tissue Distribution, and Biophysical Characterization of a Novel MammalianShaker-related Voltage-gated Potassium Channel, Kv1.7Journal of Biological Chemistry, 1998
- An Isolated Cardiac Conduction Disease Maps to Chromosome 19qCirculation Research, 1995
- Gene for Progressive Familial Heart Block Type I Maps to Chromosome 19q13Circulation, 1995
- Identity of a novel delayed rectifier current from human heart with a cloned K+ channel current.Circulation Research, 1993
- A Family of Three Mouse Potassium Channel Genes with Intronless Coding RegionsScience, 1990
- Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reactionGenomics, 1989
- Cloning of Genomic and Complementary DNA from Shaker , a Putative Potassium Channel Gene from DrosophilaScience, 1987