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  • Molecular assay reagents intended to identify deletions and duplications 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 affect many parts of the body. Genetic variants at multiple loci have been associated with Zellweger spectrum. These reagents are intended to detect deletions and duplications in the majority of Zellweger spectrum-associated loci simultaneously.
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