Extraadrenal 21-Hydroxylation by CYP2C19 and CYP3A4: Effect on 21-Hydroxylase Deficiency-Reference-Cited by-同舟云学术

Extraadrenal 21-Hydroxylation by CYP2C19 and CYP3A4: Effect on 21-Hydroxylase Deficiency

Published:2009-01-01 Issue:1 Volume:94 Page:89-95
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Gomes Larissa G.¹²,Huang Ningwu¹,Agrawal Vishal¹,Mendonça Berenice B.²,Bachega Tania A. S. S.²,Miller Walter L.¹

Affiliation:

1. Department of Pediatrics (L.G.G., N.H., V.A., W.L.M.), University of California San Francisco, San Francisco, California 94143-0978

2. Department of Endocrinology-LIM42 (L.G.G., B.B.M., T.A.S.S.B.), Hospital das Clinicas da Universidade de São Paulo, 05403-900 São Paulo, Brazil

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/94/1/89/9057143/jcem0089.pdf

Reference39 articles.

1. Results of screening 1.9 million Texas newborns for 21-hydroxylase-deficient congenital adrenal hyperplasia.;Therrell Jr;Pediatrics,1998

2. Molecular genetics of 21-hydroxylase deficiency.;Miller;Ann Rev Genet,1989

3. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency.;White;Endocr Rev,2000

4. Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia.;Dolzan;Eur J Endocrinol,2005

5. Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency.;Bachega;J Clin Endocrinol Metab,1998

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