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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943370/
https://www.ncbi.nlm.nih.gov/pubmed/29256176
http://dx.doi.org/10.1007/s00251-017-1041-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943370/
https://www.ncbi.nlm.nih.gov/pubmed/29256176
http://dx.doi.org/10.1007/s00251-017-1041-3

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