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

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.

Opis bibliograficzny
Główni autorzy: 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
Język:English
Wydane: 2001
Hasła przedmiotowe:
R5-920 Medicine (General)
Dostęp online: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

Internet

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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