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Molecular assay reagents intended to identify genetic variants 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 multiple peroxisomal disorder-associated loci simultaneously.
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