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  • Molecular assay reagents intended to identify deletions and duplications in genes 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 deletions and duplications in multiple Zellweger syndrome-associated loci simultaneously.
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