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  • Molecular assay reagents intended to identify gene variants associated with short QT syndrome, a form of cardiac arrhythmia characterized by a shortened QT interval on electrocardiogram. Genetic variants at multiple loci have been associated with short QT syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple short QT syndrome-associated loci simultaneously.
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