Yea SS, Lee SS, Kim WY, et al. (2008). „Genetic variations and haplotypes of UDP-glucuronosyltransferase 1A locus in a Korean population.”. Ther Drug Monit. 30 (1): 23—34. PMID18223459. S2CID34396409. doi:10.1097/FTD.0b013e3181633824.
van Es HH, Bout A, Liu J, et al. (1993). „Assignment of the human UDP glucuronosyltransferase gene (UGT1A1) to chromosome region 2q37”. Cytogenet. Cell Genet. 63 (2): 114—6. PMID8467709. doi:10.1159/000133513.
Gong QH, Cho JW, Huang T, et al. (2001). „Thirteen UDPglucuronosyltransferase genes are encoded at the human UGT1 gene complex locus”. Pharmacogenetics. 11 (4): 357—68. PMID11434514. doi:10.1097/00008571-200106000-00011.
Ross CJ, Katzov-Eckert H, Dubé MP, et al. (2009). „Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy”. Nat. Genet. 41 (12): 1345—9. PMID19898482. S2CID21293339. doi:10.1038/ng.478.