Whole-genome resequencing in pharmacogenomics: Moving away from past disparities to globally representative applications
dc.contributor.author | Drgemller B.I. | |
dc.contributor.author | Wright G.E.B. | |
dc.contributor.author | Niehaus D.J.H. | |
dc.contributor.author | Emsley R.A. | |
dc.contributor.author | Warnich L. | |
dc.date.accessioned | 2012-01-18T08:06:43Z | |
dc.date.available | 2012-01-18T08:06:43Z | |
dc.date.issued | 2011 | |
dc.description | Please help us populate SUNScholar with the post print version of this article. It can be e-mailed to: scholar@sun.ac.za | |
dc.identifier.citation | Pharmacogenomics | |
dc.identifier.citation | 12 | |
dc.identifier.citation | 12 | |
dc.identifier.citation | http://www.scopus.com/inward/record.url?eid=2-s2.0-82255196216&partnerID=40&md5=7c5aa909d37e4808741ccc72ccd99f47 | |
dc.identifier.issn | 14622416 | |
dc.identifier.other | 10.2217/pgs.11.119 | |
dc.identifier.uri | http://hdl.handle.net/10019.1/19308 | |
dc.subject | abacavir | |
dc.subject | cisplatin | |
dc.subject | clopidogrel | |
dc.subject | mercaptopurine | |
dc.subject | tamoxifen | |
dc.subject | warfarin | |
dc.subject | African | |
dc.subject | allele | |
dc.subject | bleeding | |
dc.subject | DRESS syndrome | |
dc.subject | ethnic group | |
dc.subject | gene frequency | |
dc.subject | gene sequence | |
dc.subject | genetic association | |
dc.subject | genetic variability | |
dc.subject | genome | |
dc.subject | genotype | |
dc.subject | hearing loss | |
dc.subject | homozygosity | |
dc.subject | human | |
dc.subject | medical research | |
dc.subject | pharmacogenomics | |
dc.subject | prediction | |
dc.subject | protein function | |
dc.subject | reliability | |
dc.subject | review | |
dc.subject | single nucleotide polymorphism | |
dc.subject | unspecified side effect | |
dc.title | Whole-genome resequencing in pharmacogenomics: Moving away from past disparities to globally representative applications | |
dc.type | Review |