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 (Health Campus) > Pusat Pengajian Sains Perubatan (School of Medical Sciences)
Depositing User:	ARKM Al Rashid Automasi
Date Deposited:	04 Jan 2009 23:49
Last Modified:	13 Jul 2013 03:37
URI:	http://eprints.usm.my/id/eprint/7245

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