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Alpha-thalassemia

what is Alpha-thalassemia source(wikipedia)

Alpha-thalassemia (α-thalassemia) is a form of thalassemia involving the genes HBA1 and HBA2. Alpha-thalassemia is due to impaired production of 1,2,3, or 4 alpha globin chains, leading to a relative excess of beta globin chains. The degree of impairment is based on which clinical phenotype is present (how many chains are affected).

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