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  • Molecular assay reagents intended to identify deletions or duplications of the uromodulin (UMOD) gene, located at chromosome 16p12.3, which encodes the protein uromodulin. Genetic variants at this locus have been associated with familial juvenile gout; glomerulocystic kidney disease with hyperuricemia and isosthenuria; and medullary cystic kidney disease.
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