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  • Molecular assay reagents intended to identify deletions or duplications of the ryanodine receptor 2 (RYR2) gene, located at chromosome 1q43, which encodes the protein ryanodine receptor 2. Genetic variants at this locus have been associated with catecholaminergic polymorphic ventricular tachycardia and familial arrhythmogenic right ventricular dysplasia.
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