The frequency of eight common point mutations in CYP21 gene in Iranian patients with congenital adrenal hyperplasia

Iranian Biomedical Journal

Volumn 12, Issue 1, 2008, Pages 49-53

  Ramazani, Ali ^a   Kahrizi, Kimia ^b   Razaghiazar, Maryam ^c   Mahdieh, Nejat ^b,d   Koppens, Paul ^e  

^a ZANJAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b UNIVERSITY OF SOCIAL WELFARE AND REHABILITATION SCIENCES   (Iran)

^c IRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^d TARBIAT MODARES UNIVERSITY   (Iran)

^e SOPHIA CHILDREN S HOSPITAL   (Netherlands)

Author keywords

Congenital adrenal hyperplasia (CAH); CYP21 gene; Mutation

Indexed keywords

STEROID 21 MONOOXYGENASE;

ALLELE; ARTICLE; CLINICAL ARTICLE; CONGENITAL ADRENAL HYPERPLASIA; CONTROLLED STUDY; ETHNICITY; EXON; GENE FREQUENCY; HUMAN; IRAN; MUTATION RATE; POINT MUTATION; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS;

ADRENAL HYPERPLASIA, CONGENITAL; HUMANS; POINT MUTATION; STEROID 21-HYDROXYLASE;

EID: 38349050416     PISSN: 1028852X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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