Steroid 21-hydroxylase deficiency and the major histocompatibility complex-Reference-Cited by-同舟云学术

Steroid 21-hydroxylase deficiency and the major histocompatibility complex

Published:1986-04 Issue:4 Volume:15 Page:404-415
ISSN:0198-8859
Container-title:Human Immunology
language:en
Short-container-title:Human Immunology

Author:

White Perrin C.,Werkmeister Janet,New Maria I.,Dupont Bo

Publisher

Elsevier BV

Subject

General Medicine,Immunology,Immunology and Allergy

Reference36 articles.

1. Dupont B: HLA and endocrine diseases. In: G. Chiumello, M. Sperling, Eds. Recent progress in pediatric endocrinology. New York, Raven Press, p. 171.

2. Inborn errors of steroid biosynthesis;Finkelstein;Physiol Rev,1979

3. Congenital adrenal hyperplasia and related conditions;New,1982

4. Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency);Dupont;Lancet,1977

5. Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage group;Levine;N Engl J Med,1978

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1. Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene;Annals of Pediatric Endocrinology & Metabolism;2024-02-29

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3. Cytochromes P450: Roles in Diseases;Journal of Biological Chemistry;2013-06

4. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Annals of the New York Academy of Sciences;2010-04

5. Identification in the HLA class I region of a gene expressed late in keratinocyte differentiation.;Proceedings of the National Academy of Sciences;1993-10-15