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. 2015 May;100(5):e169-71.
doi: 10.3324/haematol.2014.115733. Epub 2015 Jan 16.

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

Raffaella Origa  1 , Mario Cazzola  2 , Elisabetta Mereu  1 , Fabrice Danjou  1 , Susanna Barella  3 , Nicolina Giagu  3 , Renzo Galanello  1 , Dorine W Swinkels  4
Affiliations

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

Raffaella Origa et al. Haematologica. 2015 May.
No abstract available

Keywords: erythropoiesis-hepcidin-iron store axis; hemoglobin H disease; β-thalassemia intermedia.

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