Influence of βS-globin haplotypes hydrox
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Laurentino, Marília Rocha; Filho, Pedro Aurio Maia; Barbosa, Maritza Cavalcante;
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Article
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2014
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SciELO
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English
⚖ 197 KB
## Background Sickle cell anemia is a chronic inflammatory disease characterized by an increased production of proinflammatory cytokines including tumor necrosis factor-alpha. Hydroxyurea, by decreasing the polymerization of hemoglobin, reduces inflammatory states. The effect of the genetic polymor