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Major histocompatibility complex class II deficiency due to a novel mutation in RFXANK in a child of Mexican descent
MHC Class II deficiency (also known as bare lymphocyte syndrome type II) is a rare primary immunodeficiency disorder inherited in an autosomal recessive fashion resulting from the absence of MHC class II molecules on the surface of immune cells. Here, we report a now 18-month-old male born to consan...
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| Publicat a: | J Clin Immunol |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4720537/ https://ncbi.nlm.nih.gov/pubmed/26634365 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10875-015-0219-4 |
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