Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea. [electronic resource]
Producer: 20080108Description: 386-94 p. digitalISSN:- 1470-269X
- Alcohol Oxidoreductases -- genetics
- Anemia, Sickle Cell -- blood
- Antisickling Agents -- metabolism
- Arginase -- genetics
- Biotransformation -- genetics
- Chromosomes, Human, Pair 6
- Chromosomes, Human, Pair 8
- Double-Blind Method
- Erythropoiesis -- genetics
- Fetal Hemoglobin -- metabolism
- Genotype
- Humans
- Hydroxyurea -- metabolism
- Linkage Disequilibrium
- Nitric Oxide Synthase Type I -- genetics
- Phenotype
- Polymorphism, Single Nucleotide
- Severity of Illness Index
- Time Factors
- Treatment Outcome
- United States
- Vascular Endothelial Growth Factor Receptor-1 -- genetics
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Publication Type: Journal Article; Multicenter Study; Randomized Controlled Trial; Research Support, N.I.H., Extramural
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