Cardiac conduction defects associate with mutations in SCN5A
- 1 September 1999
- journal article
- Published by Springer Nature in Nature Genetics
- Vol. 23 (1), 20-21
- https://doi.org/10.1038/12618
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophyNature Genetics, 1999
- Congenital Heart Disease Caused by Mutations in the Transcription Factor NKX2-5Science, 1998
- Linkage of Familial Dilated Cardiomyopathy with Conduction Defect and Muscular Dystrophy to Chromosome 6q23American Journal of Human Genetics, 1997
- Genomic Organization of the HumanSCN5AGene Encoding the Cardiac Sodium ChannelGenomics, 1996
- Mapping a cardiomyopathy locus to chromosome 3p22-p25.Journal of Clinical Investigation, 1996
- An Isolated Cardiac Conduction Disease Maps to Chromosome 19qCirculation Research, 1995
- Gene for Progressive Familial Heart Block Type I Maps to Chromosome 19q13Circulation, 1995
- A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1–1q1Nature Genetics, 1994
- The Pathogenesis of Atrioventricular Block in Coronary DiseaseCirculation, 1970
- Etiology and pathology of bilateral bundle branch block in relation to complete heart blockProgress in Cardiovascular Diseases, 1964