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HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency.

Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21-OH-def) has been established to be an HLA-linked, recessive monogenetic disease. However, two nonclassical forms of 21-OH-def have also been described: "cryptic" 21-OH-def, which has been shown to be HLA-linked,...

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Detalhes bibliográficos
Main Authors: Pollack, M S, Levine, L S, O'Neill, G J, Pang, S, Lorenzen, F, Kohn, B, Rondanini, G F, Chiumello, G, New, M I, Dupont, B
Formato: Artigo
Idioma:Inglês
Publicado em: 1981
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1685089/
https://ncbi.nlm.nih.gov/pubmed/6789674
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