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

• Main Authors: Muhamad, Y.K., Fuziah, M.Z., Rus Anida, A., Sidek, M.Ros, Ramli, S.F., Adam, N., Isa, M.N.
• Format: Conference or Workshop Item
• Language: English
• Published: 2001
• Subjects: R5-920 Medicine (General)
• Online Access: http://eprints.usm.my/7245/1/Detection_of_point_mutation_%28pro30Leu%29_in_exon_1_of_the_21-hydroxylase_gene_%28CYP21%29_in_pattient_with_congenital_adrenal_hyperplasia_using.pdf; http://eprints.usm.my/7245/
• Institution: Universiti Sains Malaysia

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