|
?:definition
|
-
Molecular assay reagents intended to identify deletions or duplications of genes associated with long QT syndrome, a condition characterized by episodic syncope (i.e., fainting) and a prolonged QT interval on electrocardiogram. Genetic variants at multiple loci have been associated with various forms of long QT Syndrome (e.g., Romano-Ward Syndrome, Jervell-Lange Nielson Syndrome). These reagents are intended to detect deletions and duplications in the majority of long QT syndrome-associated loci simultaneously.
|
![[This page as RDF]](https://research.tib.eu/covid-19/static/rdf-icon.gif){kind=icon}