Detection Of Point Mutation (Pro30Leu) In Exon 1 Of The 21-Hydroxylase Gene(Cyp21) In Patient With Congenital
Adrenal Hyperplasia Using Digoxygenin System .
Congenital adrenal hyperplasia IS an autosomal recessive disease with a wide range of clinical manifestations.
Bibliographic Details
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
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Language: | English |
Published: |
2001
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Subjects: | |
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
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