SCOPUS 정보 검색 플랫폼

Lancet

Volumn 364, Issue 9446, 2004, Pages 1663-

P450 oxidoreductase deficiency [2]

(4) Miller, Walter L a Huang, Ningwu a Flück, Christa E b Pandey, Amit V a

a UNIVERSITY OF CALIFORNIA (United States)

b UNIVERSITY CHILDREN S HOSPITAL (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P450;

AMINO ACID SEQUENCE; ENZYME ACTIVITY; ENZYME DEFICIENCY; GENE MUTATION; HETEROZYGOSITY; LETTER; MEASUREMENT; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL;

EID: 7644240722 PISSN: 01406736 EISSN: None Source Type: Journal
DOI: 10.1016/S0140-6736(04)17344-3 Document Type: Letter

Times cited : (30)

References (4)

1
- 3042613405
- Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis: Analytical study
- Arlt W, Walker EA, Draper N, et al. Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis: analytical study. Lancet. 363:2004;2128-2135
- (2004) Lancet , vol.363 , pp. 2128-2135
- Arlt, W.¹ Walker, E.A.² Draper, N.³

2
- 10744224515
- Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome
- Flück CE, Tajima T, Pandey AV, et al. Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome. Nature Genet. 36:2004;228-230
- (2004) Nature Genet , vol.36 , pp. 228-230
- Flück, C.E.¹ Tajima, T.² Pandey, A.V.³

3
- 0031252385
- The genetic and functional basis of isolated 17,20 lyase deficiency
- Geller DG, Auchus RJ, Mendonça BB, Miller WL. The genetic and functional basis of isolated 17,20 lyase deficiency. Nature Genet. 17:1997;201-205
- (1997) Nature Genet , vol.17 , pp. 201-205
- Geller, D.G.¹ Auchus, R.J.² Mendonça, B.B.³ Miller, W.L.⁴

4
- 0032893922
- 5
- 5. Mol Endocrinol. 13:1999;167-175
- (1999) Mol Endocrinol , vol.13 , pp. 167-175
- Geller, D.G.¹ Auchus, R.J.² Miller, W.L.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.