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Molecular assay reagents intended to identify gene variants associated with glycine encephalopathy, a form of encephalopathy characterized by elevated glycine levels. Genetic variants at multiple loci have been associated with glycine encephalopathy. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple glycine encephalopathy-associated loci simultaneously.
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