Frequencies of A(TA)7TAA, G71R, and G493R mutations of the UGT1A1 gene in the Malaysian population
The A(TA)7TAA seems more common than the G71R and G493R mutations in the Malaysian population. BACKGROUND: Gilbert syndrome is caused by defects in the uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) gene. These mutations differ among different populations and many of them have been fo...
Main Authors: | Yusoff, Surini, Van Rostenberghe, Hans, Yusoff, Narazah M, A.Talib, Norlelawati, Ramli, Noraida, Ismail, N Zainal A N, Ismail, W Pauzi W, Matsuo, Masafumi, Nishio, Hisahide |
---|---|
Format: | Article |
Language: | English |
Published: |
2006
|
Subjects: | |
Online Access: | http://irep.iium.edu.my/12680/1/Surini_et.al.pdf |
Similar Items
-
Evaluation of mutation effects on UGT1A1 activity toward 17beta-estradiol using liquid chromatography-tandem mass spectrometry
by: Wada, Keiko, et al.
Published: (2006) -
Association of G71R Mutation of the UGT1A1 Gen with Neonatal Hyper Bilirubinemia in the Iranian Population
by: Ebrahim Dastgerdy, et al.
Published: (2012-03-01) -
The Association between Prolonged Jaundice and UGT1A1 Gene Polymorphism (G71R) in Gilbert's Syndrome
by: Ehsan Alaee, et al.
Published: (2016-11-01) -
Bilirubin - Uridine Diphosphate
Glucuronosyltransferase (Ugt1a1)
Gene Mutations Among Newborn Babies
In The Malay Population In Kelantan
With Hyperbilirubinaemia
by: Yusoff, Surini
Published: (2005) -
Human Dystrophin Dp71ab Enhances the Proliferation of Myoblasts Across Species But Not Human Nonmyoblast Cells
by: Manal Farea, et al.
Published: (2022-04-01)