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Effects of α-tocopherol on hemolysis and oxidative stress markers on red blood cells in β-thalassemia major

Sovira N, Lubis M, Wahidiyat PA, Suyatna FD, Gatot D, Bardosono S, Sadikin M

Background: The accumulation of unpaired α-globin chains in patients with β-thalassemia major may clinically create ineffective erythropoiesis, hemolysis, and chronic anemia. Multiple blood transfusions and iron overload cause cellular oxidative...
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