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

Raffaella Origa, Mario Cazzola, Elisabetta Mereu, Fabrice Danjou, Susanna Barella, Nicolina Giagu, Renzo Galanello, Dorine W. Swinkels

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)e169-e171
JournalHaematologica
Volume100
Issue number5
DOIs
Publication statusPublished - 2015

Keywords

  • Erythropoiesis-hepcidin-iron store axis
  • Hemoglobin H disease
  • β-thalassemia intermedia

ASJC Scopus subject areas

  • Hematology

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