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  • Molecular assay reagents intended to identify genetic variants associated with urea cycle disorders, a collection of genetic disorders caused by deficiencies in waste nitrogen metabolism. Genetic variants at multiple loci have been associated with urea cycle disorders. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple urea cycle disorder-associated loci simultaneously.
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