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