A novel pattern of uridine diphosphate glucuronosyltransferase polymorphisms associated with hyperbilirubinemia during nilotinib treatment

Blood Cells Mol Dis. 2013 Oct;51(3):162. doi: 10.1016/j.bcmd.2013.05.007. Epub 2013 Jun 13.

Authors

Claudio Fozza, Simonetta Pardini, Alessandra Coiana, Maria Cristina Rosatelli, Maurizio Longinotti

PMID: 23769327
DOI: 10.1016/j.bcmd.2013.05.007

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Adult
Genotype
Glucuronosyltransferase / genetics*
Humans
Hyperbilirubinemia / chemically induced
Hyperbilirubinemia / genetics*
Leukemia, Myelogenous, Chronic, BCR-ABL Positive / complications
Leukemia, Myelogenous, Chronic, BCR-ABL Positive / drug therapy
Male
Polymorphism, Genetic
Pyrimidines / adverse effects
Pyrimidines / therapeutic use

Substances

Pyrimidines
Glucuronosyltransferase
nilotinib