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  • Molecular assay reagents intended to identify deletions or duplications of the desmoglein 2 (DSG2) gene, located at chromosome 18q12.1, which encodes the protein desmoglein-2. Genetic variants at this locus have been associated with dilated cardiomyopathy 1bb, arrhythmogenic right ventricular cardiomyopathy, type 10, and primary dilated cardiomyopathy.
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