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Study of Bil-Uridine Diphosphate Glucuronyl Transferase (BILUDGPT- 1) Mutation in Neonatal Hyperbilirubinaemia with Glucose-6-Phosphate Dehydrogenase Deficiency.

Mohd Yusoff, Dr Narazah Study of Bil-Uridine Diphosphate Glucuronyl Transferase (BILUDGPT- 1) Mutation in Neonatal Hyperbilirubinaemia with Glucose-6-Phosphate Dehydrogenase Deficiency. Project Report. Universiti Sains Malaysia.

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Abstract

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 found to be genetic risk factors for the development of neonatal jaundice.

Item Type:Monograph (Project Report)
Subjects:R Medicine > R Medicine (General) > R735-854 Medical education. Medical schools. Research
ID Code:10885
Deposited By:Mr Erwan Roslan
Deposited On:06 Jul 2009 11:58
Last Modified:06 Jul 2009 11:58

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