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Peer-reviewed veterinary case report

Erythroferrone: the missing link in β-thalassemia?

Journal:
Blood
Year:
2015
Authors:
Moura, Ivan C & Hermine, Olivier
Affiliation:
IMAGINE INSTITUTE.
Species:
rodent

Abstract

In this issue of Blood, Kautz et al show that the ablation of the erythroid-derived factor erythroferrone (ERFE), which has been shown to be highly expressed in β-thalassemic mice, restores hepcidin levels and corrects iron overload. However, correction of hepcidin levels in those mice does not improve anemia of β-thalassemia.

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Original publication: https://pubmed.ncbi.nlm.nih.gov/26494918/