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  • Molecular assay reagents intended to identify variants in the majority of genes known to be associated with peroxisomal disorders, a collection of genetic diseases associated with deficiencies in peroxisome function or biogenesis. Genetic variants at multiple loci have been associated with peroxisomal disorders. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in the majority of peroxisomal disorder-associated loci simultaneously.
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