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  • Molecular assay reagents intended to identify mutations in the hemoglobin, beta (HBB) gene, located at chromosome 11p15.5, which encodes for beta chain of hemoglobin. Mutations at this locus have been identified in patients with a group of symptomatic disorders characterized by the presence of hemoglobin S (Hb S), especially sickle cell anemia (Hb SS); they are also associated with sickle-hemoglobin C disease (Hb SC) and with two types of sickle beta-thalassemia.
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