Susceptibility to mycobacterial disease due to mutations in IL-12Rβ1 in three Iranian patients

In the last decade, autosomal recessive interleukin-12 receptor β1 (IL-12Rβ1) deficiency, the most common cause of Mendelian susceptibility to mycobacterial disease (MSMD), has been diagnosed in a few children and adults with severe tuberculosis in Iran. Here, we report three cases referred to the I...

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Detalhes bibliográficos
Publicado no:Immunogenetics
Main Authors: Alinejad Dizaj, Maryam, Mortaz, Esmaeil, Mahdaviani, Seyed Alireza, Mansouri, Davood, Mehrian, Payam, Verhard, Els M., Varahram, Mohammad, Babaie, Delara, Adcock, Ian M., Garssen, Johan, van de Vosse, Esther, Velayati, Aliakbar
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2017
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5943370/
https://ncbi.nlm.nih.gov/pubmed/29256176
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00251-017-1041-3
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