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Volumn 48, Issue 6, 2002, Pages 818-825

Multiplex minisequencing of the 21-hydroxylase gene as a rapid strategy to confirm congenital adrenal hyperplasia

Author keywords

[No Author keywords available]

Indexed keywords

STEROID 21 MONOOXYGENASE;

EID: 0036274380     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1093/clinchem/48.6.818     Document Type: Article
Times cited : (63)

References (36)
  • 6
    • 0031910562 scopus 로고    scopus 로고
    • Molecular genetics of congenital adrenal hyperplasia (21-hydroxylase deficiency): Implications for diagnosis, prognosis and treatment
    • (1998) Acta Paediatr , vol.87 , pp. 159-164
    • Wedell, A.1
  • 28
    • 0027215606 scopus 로고
    • Steroid 21-hydroxylase (P450c21): A new allele and spread of mutations through the pseudogene
    • (1993) Hum Genet , vol.91 , pp. 236-240
    • Wedell, A.1    Luthman, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.