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dc.contributor.authorWadley, A.
dc.contributor.authorLombard, Z.
dc.contributor.authorCherry, C.
dc.contributor.authorPrice, Patricia
dc.contributor.authorKamerman, P.
dc.date.accessioned2017-01-30T13:51:15Z
dc.date.available2017-01-30T13:51:15Z
dc.date.created2015-10-29T04:10:06Z
dc.date.issued2012
dc.identifier.citationWadley, A. and Lombard, Z. and Cherry, C. and Price, P. and Kamerman, P. 2012. Analysis of a previously identified "pain-protective" haplotype and individual polymorphisms in the GCH1 gene in Africans with HIV-associated sensory neuropathy: A genetic association study. Journal of Acquired Immune Deficiency Syndromes. 60 (1): pp. 20-23.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/35713
dc.identifier.doi10.1097/QAI.0b013e31824bcc17
dc.description.abstract

We analyzed GTP cyclohydrolase 1 in symptomatic HIV-associated sensory neuropathy in Southern Africans including a "painprotective" 3-SNP haplotype and 6 SNPs, analyzed individually and in a 6-SNP haplotype. The "pain-protective" 3-SNP haplotype and a 6-SNP haplotype containing these alleles associated with a reduced risk of pain. Another 3-SNP haplotype associated with increased presence of pain. Associations were lost after correction for age, gender, and CD4 T-cell count. Linkage disequilibrium differed between our cohort and Caucasians suggesting that these SNPs may not be ideal markers in Africans. Subsequently, the role of GTP cyclohydrolase 1 in painful HIV-associated sensory neuropathy remains possible. Copyright © 2012 by Lippincott Williams & Wilkins.

dc.titleAnalysis of a previously identified "pain-protective" haplotype and individual polymorphisms in the GCH1 gene in Africans with HIV-associated sensory neuropathy: A genetic association study
dc.typeJournal Article
dcterms.source.volume60
dcterms.source.number1
dcterms.source.startPage20
dcterms.source.endPage23
dcterms.source.issn1525-4135
dcterms.source.titleJournal of Acquired Immune Deficiency Syndromes
curtin.departmentSchool of Biomedical Sciences
curtin.accessStatusOpen access via publisher


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