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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
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 |
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