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Volumn 87, Issue 6, 2002, Pages 2824-2829

Novel mutations in CYP21 detected in individuals with hyperandrogenism

Author keywords

[No Author keywords available]

Indexed keywords

HYDROXYPROGESTERONE; PROGESTERONE;

EID: 0036072224     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.87.6.2824     Document Type: Article
Times cited : (47)

References (35)
  • 2
    • 0022273224 scopus 로고
    • Clinical and endocrinological aspects of 21-hydroxylase deficiency
    • (1985) Ann NY Acad Sci , vol.458 , pp. 1-27
    • New, M.I.1
  • 7
    • 0032053606 scopus 로고    scopus 로고
    • Identification of heterozygotic carriers of 21-hydroxylase deficiency: Sensitivity of ACTH stimulation tests
    • (1998) Am J Med Genet , vol.76 , pp. 337-342
    • Witchel, S.F.1    Lee, P.A.2
  • 14
  • 15
    • 0028063901 scopus 로고
    • A steroid 21-hydroxylase allele concomitantly carrying four disease-causing mutations is not uncommon in the Swedish population
    • (1994) Hum Genet , vol.93 , pp. 204-206
    • Wedell, A.1    Xu, C.2    Luthman, H.3
  • 34
    • 0034112647 scopus 로고    scopus 로고
    • A 3D model of human P450c21: Study of the putative effects of steroid 21-hydroxylase gene mutations
    • (2000) Hum Genet , vol.106 , pp. 3309-3339
    • Mornet, E.1    Gibrat, J.-F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.