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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Pubblicato in:Immunogenetics
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: Springer Berlin Heidelberg 2017
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Original Article
Accesso online: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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