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  • Molecular assay reagents intended to identify deletions and duplications in genes associated with metachromatic leukodystrophy, a genetic disorder affecting lipid metabolism and characterized by the accumulation of sulfatides, which leds to progressive white matter loss throughout the nervous system. Genetic variants at multiple loci have been associated with metachromatic leukodystrophy. These reagents are intended to detect deletions and duplications in multiple metachromatic leukodystrophy-associated loci simultaneously.
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