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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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Detalhes bibliográficos
Publicado no:J Clin Immunol
Main Authors: Clarridge, Katherine, Leitenberg, David, Loechelt, Brett, Picard, Capuchine, Keller, Michael
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
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Acesso em linha: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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