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Loss of α hemoglobin–stabilizing protein impairs erythropoiesis and exacerbates β thalassemia

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Figure

Figure 1) Prussian blue staining for cellular iron in spleen. Increased iron in AHSP–/– spleen reflects accelerated clearance of erythroid cells by the reticuloendothelial system
Figure 2Erythroid hyperplasia in
Figure 4Unstable hemoglobins in
Figure 6AHSP prevents
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