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

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

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.

Bibliographic Details
Main Author:	Mohd Yusoff, Dr Narazah
Format:	Monograph
Language:	English
Published:	Universiti Sains Malaysia 2005
Subjects:	R735-854 Medical education. Medical schools. Research
Online Access:	http://eprints.usm.my/10885/ http://eprints.usm.my/10885/1/Study%20of%20Bil-Uridine%20Diphosphate%20Glucuronyl%20Transferase.pdf

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