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.

[img]
Preview
PDF
Download (2060Kb) | Preview

    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
    Divisions: Institut Perubatan & Pergigian Termaju (Advanced Medical & Dental Institute)
    Depositing User: Mr Erwan Roslan
    Date Deposited: 06 Jul 2009 11:58
    Last Modified: 13 Jul 2013 12:32
    URI: http://eprints.usm.my/id/eprint/10885

    Actions (login required)

    View Item
    Share