Genetic linkage of hyper-IgE syndrome to chromosome 4.

The hyper-IgE syndrome (HIES) is a rare primary immunodeficiency characterized by recurrent skin abscesses, pneumonia, and highly elevated levels of serum IgE. HIES is now recognized as a multisystem disorder, with nonimmunologic abnormalities of the dentition, bones, and connective tissue. HIES can...

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Detalhes bibliográficos
Main Authors: Grimbacher, B, Schäffer, A A, Holland, S M, Davis, J, Gallin, J I, Malech, H L, Atkinson, T P, Belohradsky, B H, Buckley, R H, Cossu, F, Español, T, Garty, B Z, Matamoros, N, Myers, L A, Nelson, R P, Ochs, H D, Renner, E D, Wellinghausen, N, Puck, J M
Formato: Artigo
Idioma:Inglês
Publicado em: 1999
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377980/
https://ncbi.nlm.nih.gov/pubmed/10441580
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