Long QT Syndrome 1
Description
An autosomal dominant condition caused by mutation(s) in the KCNQ1 gene, encoding potassium voltage-gated channel subfamily KQT member 1. It is characterized by a prolonged QT interval that may result in torsade de pointes, ventricular fibrillation and/or sudden cardiac death.
Cell Lines
- LUMCi039-A
- MRIi005-A
- NUIGi005-A
- NUIGi005-B
- NUIGi005-C
- NUIGi006-A
- NUIGi006-B
- NUIGi006-C
- NUIGi007-A
- NUIGi007-B
- NUIGi008-A
- NUIGi008-B
- NUIGi008-C
- NUIGi009-A
- NUIGi009-B
- NUIGi009-C
- NUIGi010-A
- NUIGi010-B
- NUIGi010-C
- NUIGi011-A
- NUIGi011-B
- NUIGi011-C
- SCVIi110-A
- SCVIi111-A
- TAUi006-A
- TAUi006-B
- TAUi007-A
- TAUi007-B
- WAe009-A-1D
- WAe009-A-62
- WAe009-A-79