Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermedia - Origa, R.; Cazzola, M.; Mereu, E.; Danjou, F.; Barella, S.; Giagu, N.; Galanello, R.; Swinkels, D. W. (Haematologica (Roma), 2015)