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  • Molecular assay reagents intended to identify genetic variants associated with Sanfilippo syndrome, a genetic disease caused by deficiencies in heparin sulfate metabolism. Genetic variants at multiple loci have been associated with Sanfilippo syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Sanfilippo syndrome-associated loci simultaneously.
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