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The immunological detection of a 21-OH deficiency mutation HLA supratype.

Previous studies have shown that the late-onset and cryptic forms of 21-hydroxylase deficiency are highly associated with the HLA supratype HLA-B14,C4A2,C4B1/2,DR1. Since cells from a number of unrelated normal individuals from different ethnic backgrounds expressing the DR1 associated with this sup...

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Detalles Bibliográficos
Main Authors: Pollack, M S, Keenan, B, Christiansen, F T, Cobain, T J, Dawkins, R L, Clayton, G
Formato: Artigo
Idioma:Inglês
Publicado: 1986
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1684832/
https://ncbi.nlm.nih.gov/pubmed/3013005
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