LRBA in the endomembrane system
Bi-allelic mutations in LRBA (from Lipopolysaccharide-responsive and beige-like anchor protein) result in a primary immunodeficiency with clinical features ranging from hypogammaglobulinemia and lymphoproliferative syndrome to inflammatory bowel disease and heterogeneous autoimmune manifestations. L...
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| Publicado no: | Colombia Médica |
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| Principais autores: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Universidad del Valle
2018
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| Assuntos: | |
| Acesso em linha: | https://www.redalyc.org/articulo.oa?id=28357492008 https://www.redalyc.org/journal/283/28357492008/ https://www.redalyc.org/journal/283/28357492008/html/ https://www.redalyc.org/journal/283/28357492008/28357492008.epub https://www.redalyc.org/journal/283/28357492008/movil |
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