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  • Molecular assay reagents intended to identify genetic variants associated with Neimann-Pick disease, a collection of genetic disorders characterized by the accumulation of lipids and cholesterol in various tissues. Genetic variants at multiple loci have been associated with Neimann-Pick disease. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Neimann-Pick disease-associated loci simultaneously.
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