dc.contributor.author | AYDOGMUS, Cigdem | |
dc.contributor.author | HASSANI, Amal | |
dc.contributor.author | NOLAN, Daniel | |
dc.contributor.author | NAJIB, Jilali | |
dc.contributor.author | Hatipoglu, Nevin | |
dc.contributor.author | TANIR, Gonul | |
dc.contributor.author | AYTEKIN, Caner | |
dc.contributor.author | Aksu, Guside | |
dc.contributor.author | Kutukculer, Necil | |
dc.contributor.author | Mansouri, Davood | |
dc.contributor.author | BUSTAMANTE, Jacinta | |
dc.contributor.author | FEINBERG, Jacqueline | |
dc.contributor.author | SAMARINA, Arina | |
dc.contributor.author | GRANT, Audrey V. | |
dc.contributor.author | BOISSON-DUPUIS, Stephanie | |
dc.contributor.author | PARVANEH, Nima | |
dc.contributor.author | BOUSFIHA, Aziz | |
dc.contributor.author | MAHDAVIANI, Alireza | |
dc.contributor.author | MAMISHI, Setareh | |
dc.contributor.author | ALCAIS, Alexandre | |
dc.contributor.author | ABEL, Laurent | |
dc.contributor.author | CASANOVA, Jean-Laurent | |
dc.contributor.author | Keser, Melike | |
dc.contributor.author | Camcioglu, Yildiz | |
dc.contributor.author | Somer, Ayper | |
dc.contributor.author | EL BAGHDADI, Jamila | |
dc.contributor.author | JANNIERE, Lucile | |
dc.contributor.author | EL HAFIDI, Naima | |
dc.date.accessioned | 2021-03-03T18:55:06Z | |
dc.date.available | 2021-03-03T18:55:06Z | |
dc.date.issued | 2011 | |
dc.identifier.citation | BOISSON-DUPUIS S., EL BAGHDADI J., PARVANEH N., BOUSFIHA A., BUSTAMANTE J., FEINBERG J., SAMARINA A., GRANT A. V. , JANNIERE L., EL HAFIDI N., et al., "IL-12R beta 1 Deficiency in Two of Fifty Children with Severe Tuberculosis from Iran, Morocco, and Turkey", PLOS ONE, cilt.6, sa.4, 2011 | |
dc.identifier.issn | 1932-6203 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_51b60c73-77a1-4617-8a7b-78584250116b | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/58071 | |
dc.identifier.uri | https://doi.org/10.1371/journal.pone.0018524 | |
dc.description.abstract | Background and Objectives: In the last decade, autosomal recessive IL-12R beta 11 deficiency has been diagnosed in four children with severe tuberculosis from three unrelated families from Morocco, Spain, and Turkey, providing proof-of-principle that tuberculosis in otherwise healthy children may result from single-gene inborn errors of immunity. We aimed to estimate the fraction of children developing severe tuberculosis due to IL-12R beta 1 deficiency in areas endemic for tuberculosis and where parental consanguinity is common. | |
dc.language.iso | eng | |
dc.subject | Temel Bilimler | |
dc.subject | ÇOK DİSİPLİNLİ BİLİMLER | |
dc.subject | Doğa Bilimleri Genel | |
dc.subject | Temel Bilimler (SCI) | |
dc.title | IL-12R beta 1 Deficiency in Two of Fifty Children with Severe Tuberculosis from Iran, Morocco, and Turkey | |
dc.type | Makale | |
dc.relation.journal | PLOS ONE | |
dc.contributor.department | Mil Hosp Mohamed V , , | |
dc.identifier.volume | 6 | |
dc.identifier.issue | 4 | |
dc.contributor.firstauthorID | 38746 | |