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,...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
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
Format: Artigo
Sprog:Inglês
Udgivet: 1981
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1685089/
https://ncbi.nlm.nih.gov/pubmed/6789674
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker