Bilirubin-uridine diphosphate glucuronosyltransferase (UGT1A1) gene mutations among newborn babies in the Malay population in Kelantan with hyperbilirubinaemia [RJ276. S961 2005 f rb].

Yusoff, Surini (2005) Bilirubin-uridine diphosphate glucuronosyltransferase (UGT1A1) gene mutations among newborn babies in the Malay population in Kelantan with hyperbilirubinaemia [RJ276. S961 2005 f rb]. Masters thesis, Universiti Sains Malaysia.

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    Abstract

    Sindrom Gilbert berpunca daripada keabnormalan pada gen uridine diphosphate-glucuronosyltransferase 1A1 (UGT1A1) yang disebabkan oleh mutasi. Gilbert syndrome is caused by defects in the uridine diphosphateglucuronosyltransferase 1A1 (UGT1A1) gene.

    Item Type: Thesis (Masters)
    Subjects: R Medicine > RJ Pediatrics > RJ251-325 Newborn infants Including physiology, care, treatment, diseases
    Divisions: Kampus Kesihatan (Medical Campus) > Pusat Pengajian Sains Perubatan (School of Medical Sciences)
    Depositing User: ARKM Al Rashid Automasi
    Date Deposited: 16 Mar 2009 20:17
    Last Modified: 13 Jul 2013 11:54
    URI: http://eprints.usm.my/id/eprint/8475

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