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

Jones, Emma

Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait. [electronic resource] - Blood Jan 2015 - 873-80 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1528-0020

10.1182/blood-2014-10-606491 doi


Adolescent
Adult
Carrier State
Case-Control Studies
Child
Child, Preschool
Erythropoiesis--genetics
Female
Gene Expression Regulation
Genotype
Hemoglobin E--genetics
Hepcidins--genetics
Humans
Iron--metabolism
Iron Overload--etiology
Linear Models
Male
Middle Aged
Mutation
Phenotype
Severity of Illness Index
Sri Lanka
Transfusion Reaction
beta-Globins--genetics
beta-Thalassemia--genetics