Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermedia

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Bibliographic Details
Published in:	Haematologica (Roma) Vol. 100; no. 5; pp. e169 - e171
Main Authors:	Origa, R., Cazzola, M., Mereu, E., Danjou, F., Barella, S., Giagu, N., Galanello, R., Swinkels, D. W.
Format:	Journal Article
Language:	English
Published:	Italy Ferrata Storti Foundation 01.05.2015
Subjects:	alpha-Thalassemia - blood alpha-Thalassemia - diagnosis alpha-Thalassemia - metabolism beta-Thalassemia - blood beta-Thalassemia - diagnosis beta-Thalassemia - metabolism Erythropoiesis Growth Differentiation Factor 15 - blood Growth Differentiation Factor 15 - metabolism Hemolysis Hepcidins - blood Hepcidins - metabolism Humans Iron - metabolism Iron Overload - metabolism Online Only hemoglobin H disease β-thalassemia intermedia erythropoiesis-hepcidin-iron store axis
ISSN:	0390-6078, 1592-8721, 1592-8721
Online Access:	Get full text
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