2022
DOI: 10.1080/03630269.2022.2083968
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A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 Levels

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“…Thalassemia is a usual cause of microcytic hypochromic anemia, which occurs because of diminishing or lack of synthesis of the globin chain in hemoglobin [ 1 ]. This is dissimilar from other hemoglobinopathies, such as sickle cell disease, which are anatomic defects of hemoglobin [ 2 ].…”
Section: Introductionmentioning
confidence: 99%
“…Thalassemia is a usual cause of microcytic hypochromic anemia, which occurs because of diminishing or lack of synthesis of the globin chain in hemoglobin [ 1 ]. This is dissimilar from other hemoglobinopathies, such as sickle cell disease, which are anatomic defects of hemoglobin [ 2 ].…”
Section: Introductionmentioning
confidence: 99%