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  • Molecular assay reagents intended to identify gene variants associated with atypical hemolytic uremic syndrome, a disorder characterized by the formation of thrombi in the small blood vessels, particularly in the kidneys, which may lead to anemia, thrombocytopenia, and/or kidney failure. Genetic variants at multiple loci have been associated with atypical hemolytic uremic syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple atypical hemolytic uremic syndrome-associated loci simultaneously.
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