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Molecular assay reagents intended to identify gene variants in the majority of genes known to be associated with hemolytic anemia, a collection of conditions in which red blood cell destruction outpaces their production. Genetic variants at multiple loci have been associated with hemolytic anemia. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in the majority of hemolytic anemia-associated loci simultaneously.
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