Chronic inflammatory state in sickle cell anemia patients is associated with HBB(*)S haplotype. [electronic resource]
Producer: 20140911Description: 217-21 p. digitalISSN:- 1096-0023
- Adult
- Aged
- Anemia, Sickle Cell -- blood
- Case-Control Studies
- Chromosomes, Human -- genetics
- Chronic Disease
- Cytokines -- blood
- Female
- Genetic Association Studies
- Genetic Predisposition to Disease
- Haplotypes -- genetics
- Humans
- Hydroxyurea -- therapeutic use
- Inflammation -- blood
- Male
- Middle Aged
- Multigene Family
- Young Adult
- beta-Globins -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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