Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait.

Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait.

HbE β-thalassemia is the most common severe thalassemia syndrome across Asia, and millions are carriers. Clinical heterogeneity in HbE β-thalassemia is incompletely explained by genotype, and the interaction of phenotypic variation with hepcidin is unknown. The effect of thalassemia carriage on hepc...

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Príomhchruthaitheoirí: Jones, E, Pasricha, SR, Allen, A, Evans, P, Fisher, C, Wray, K, Premawardhena, A, Bandara, D, Perera, A, Webster, C, Sturges, P, Olivieri, N, St Pierre, T, Armitage, A, Porter, J, Weatherall, D, Drakesmith, H
Formáid: Journal article
Teanga:English
Foilsithe / Cruthaithe: 2014

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