Effects of α-tocopherol on hemolysis and oxidative stress markers on red blood cells in β-thalassemia major
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 damage. However, α-tocopherol, an antioxidant, is a pot...
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The Korean Pediatric Society,
2020-08-01T00:00:00Z.
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