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  • Molecular assay reagents intended to identify genetic variants associated with Zellweger spectrum, a collection of peroxisomal disorders (including infantile Refsum disease, neonatal adrenoleukodystrophy, and Zellweger syndrome) that affect many parts of the body. Genetic variants at multiple loci have been associated Zellweger spectrum. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Zellweger spectrum-associated loci simultaneously.
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