Apparent Manifesting Heterozygosity in P450 Oxidoreductase Deficiency and Its Effect on Coexisting 21-Hydroxylase Deficiency-Reference-Cited by-同舟云学术

Apparent Manifesting Heterozygosity in P450 Oxidoreductase Deficiency and Its Effect on Coexisting 21-Hydroxylase Deficiency

Published:2007-06-01 Issue:6 Volume:92 Page:2318-2322
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Scott Rachel R.¹²,Gomes Larissa G.¹,Huang Ningwu¹,Van Vliet Guy²,Miller Walter L.¹

Affiliation:

1. Division of Endocrinology (R.R.S., L.G.G., N.H., W.L.M.), Department of Pediatrics, University of California, San Francisco, San Francisco, California 94143

2. Endocrinology Service and Research Center (R.R.S., G.V.V.), Sainte-Justine Hospital, and Department of Pediatrics, University of Montreal, Montreal, Canada H3T 1C5

Publisher

The Endocrine Society

Subject

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

Link

http://academic.oup.com/jcem/article-pdf/92/6/2318/10780587/jcem2318.pdf

Reference36 articles.

1. Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome.;Flück;Nat Genet,2004

2. Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis: analytical study.;Arlt;Lancet,2004

3. P450 oxidoreductase deficiency. A new disorder of steroidogenesis with multiple clinical manifestations.;Miller;Trends Endocrinol Metab,2004

4. Regulation of steroidogenesis by electron transfer.;Miller;Endocrinology,2005

5. Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases: a new variant of congenital adrenal hyperplasia.;Peterson;N Engl J Med,1985

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