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dc.contributor.authorWere, T
dc.contributor.authorAwandare, GA
dc.contributor.authorMartinson, JJ
dc.contributor.authorOuma, C
dc.contributor.authorDavenport, GC
dc.contributor.authorOng'echa, JM
dc.contributor.authorWang, W
dc.contributor.authorL, Leng
dc.contributor.authorRE, Ferrell,
dc.contributor.authorR, Bucala,
dc.contributor.authorDJ, Perkins
dc.date.accessioned2018-01-24T13:03:23Z
dc.date.available2018-01-24T13:03:23Z
dc.date.issued2012
dc.identifier.urihttps://repository.maseno.ac.ke/handle/123456789/248
dc.description.abstractSevere malarial anemia (SMA) resulting from Plasmodium falciparum infection is one of the leading causes of childhood mortality in sub-Saharan Africa. The innate immune mediator macrophage migration inhibitory factor (MIF) plays a critical role in the pathogenesis of SMA. METHODS: To investigate the influence of MIF genetic variation on susceptibility to SMA, haplotypes of the MIF-173G/C and-794CATT5-8 polymorphisms were examined in a cohort of Kenyan children. RESULTS: A statistically significant relationship between increasing frequencies of longer CATT repeats at-794 and increasing severity of malarial anemia was observed. In addition, there was a strong association between lower MIF concentrations and longer CATT repeats. Multivariate logistic regression analyses demonstrated that the 6G haplotype (ie, MIF-794CATT6/-173G) was associated …en_US
dc.publisherJournal of Infectious Diseasesen_US
dc.titleMIF (macrophage migration inhibitory factor) promoter polymorphisms and susceptibility to severe malarial anemiaen_US
dc.typeArticleen_US


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