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