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  • Molecular assay reagents intended to identify gene variants associated with alpha thalassemia, a form of hemolytic anemia caused by defects in the hemoglobin alpha chains. Genetic variants at multiple loci have been associated with alpha thalassemia. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple alpha thalassemia-associated loci simultaneously.
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