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  • Molecular assay reagents intended to identify genetic variants associated with Zellweger syndrome, a genetic disease in the Zellweger spectrum characterized by muscle weakness, feeding problems, hearing/vision loss, seizures, and other symptoms. Genetic variants at multiple loci have been associated with Zellweger syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Zellweger syndrome-associated loci simultaneously.
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