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Regulation of Iron Absorption in Hemoglobinopathies

Beta-thalassemia and sickle cell anemia (SCD) represent the most common hemoglobinopathies caused, respectively, by deficient production or alteration of the beta chain of hemoglobin (Hb). Patients affected by the most severe form of thalassemia suffer from profound anemia that requires chronic bloo...

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Autors principals: Rechavi, Gideon, Rivella, Stefano
Format: Artigo
Idioma:Inglês
Publicat: 2008
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3722362/
https://ncbi.nlm.nih.gov/pubmed/18991651
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