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  • Molecular assay reagents intended to identify mutations in the majority of genes known to be associated with Zellweger spectrum, a collection of peroxisomal disorders (including infantile Refsum disease, neonatal adrenoleukodystrophy, and Zellweger syndrome) that effect many parts of the body. Genetic variants at multiple loci have been associated with Zellweger spectrum. These reagents are intended to detect mutations in the majority of Zellweger spectrum-associated loci simultaneously.
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