Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: A new Allele at the 21-hydroxylase locus-Reference-Cited by-同舟云学术

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Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: A new Allele at the 21-hydroxylase locus

Published:1980-07 Issue:1 Volume:1 Page:55-66
ISSN:0198-8859
Container-title:Human Immunology
language:en
Short-container-title:Human Immunology

Author:

Laron Z.,Pollack M.S.,Zamir R.,Roitman A.,Dickerman Z.,Levine L.S.,Lorenzen F.,O'Neill G.J.,Pang S.,New M.I.,Dupont B.

Publisher

Elsevier BV

Subject

General Medicine,Immunology,Immunology and Allergy

Reference25 articles.

1. Mendelian Inheritance in Man;McKusick,1975

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

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

4. HLA and congenital adrenal hyperplasia linkage confirmed;Price;Lancet,1978

5. HLA and congenital adrenal hyperplasia linkage confirmed;Weitkamp;Lancet,1978

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1. Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency;Genetic Steroid Disorders;2023

2. Adrenal Insufficiency;Pediatrics in Review;2015-03

3. Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency;Genetic Steroid Disorders;2014

4. Genetic Disorders of the Adrenal Gland;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

5. The gene founder effect of two spontaneous mutations in ethnic Chinese (Taiwanese) CAH patients with 21-hydroxylase deficiency;Molecular Genetics and Metabolism;2009-05

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