Detection Of Point Mutation (Pro30Leu) In Exon 1 Of The 21-Hydroxylase Gene(Cyp21) In Patient With Congenital Adrenal Hyperplasia Using Digoxygenin System .

Muhamad, Y.K. and Fuziah, M.Z. and Rus Anida, A. and Sidek, M.Ros and Ramli, S.F. and Adam, N. and Isa, M.N. (2001) Detection Of Point Mutation (Pro30Leu) In Exon 1 Of The 21-Hydroxylase Gene(Cyp21) In Patient With Congenital Adrenal Hyperplasia Using Digoxygenin System . In: 13th National Biotechnology Seminar , 10-13th November 2001, Bayview Hotel Pulau Pinang .

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    Abstract

    Congenital adrenal hyperplasia IS an autosomal recessive disease with a wide range of clinical manifestations.

    Item Type: Conference or Workshop Item (Paper)
    Subjects: R Medicine > R Medicine (General) > R5-920 Medicine (General)
    Divisions: Kampus Kesihatan (Medical Campus) > Pusat Pengajian Sains Perubatan (School of Medical Sciences)
    Depositing User: ARKM Al Rashid Automasi
    Date Deposited: 05 Jan 2009 07:49
    Last Modified: 13 Jul 2013 11:37
    URI: http://eprints.usm.my/id/eprint/7245

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