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S. Voskou et al.
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Rajasekhar N. V. S. Suragani et al.
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Maria C. Bonaccorsi di Patti et al.
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Leon Kautz et al.
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Paul J. Schmidt et al.
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Transfusion suppresses erythropoiesis and increases hepcidin in adult patients with β-thalassemia major: a longitudinal study
Sant-Rayn Pasricha et al.
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Jing Liu et al.
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Sheila A. Anderson et al.
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Shuling Guo et al.
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Bo Qiao et al.
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Gloria C. Preza et al.
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Jim J. Xiao et al.
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Sara Gardenghi et al.
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Transferrin therapy ameliorates disease in β-thalassemic mice
Huihui Li et al.
NATURE MEDICINE (2010)
High nontransferrin bound iron levels and heart disease in thalassemia major
Antonio Piga et al.
AMERICAN JOURNAL OF HEMATOLOGY (2009)
Controlling alpha-globin: a review of alpha-globin expression and its impact on beta-thalassemia
Hsiao Phin Joanna Voon et al.
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL (2008)
Essential role for Nix in autophagic maturation of erythroid cells
Hector Sandoval et al.
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Xiang Yu et al.
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E Nemeth et al.
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A Donovan et al.
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AT McKie et al.
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Oxidation and erythrocyte senescence
CR Kiefer et al.
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