Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait. [electronic resource]
Producer: 20150413Description: 873-80 p. digitalISSN:- 1528-0020
- 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
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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