IL-12Rβ1 deficiency in two of fifty children with severe tuberculosis from Iran, Morocco, and Turkey

In the last decade, autosomal recessive IL-12Rβ1 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 erro...

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Veröffentlicht in:PloS one 2011-04, Vol.6 (4), p.e18524
Hauptverfasser: Boisson-Dupuis, Stéphanie, El Baghdadi, Jamila, Parvaneh, Nima, Bousfiha, Aziz, Bustamante, Jacinta, Feinberg, Jacqueline, Samarina, Arina, Grant, Audrey V, Janniere, Lucile, El Hafidi, Naima, Hassani, Amal, Nolan, Daniel, Najib, Jilali, Camcioglu, Yildiz, Hatipoglu, Nevin, Aydogmus, Cigdem, Tanir, Gonul, Aytekin, Caner, Keser, Melike, Somer, Ayper, Aksu, Guside, Kutukculer, Necil, Mansouri, Davood, Mahdaviani, Alireza, Mamishi, Setareh, Alcais, Alexandre, Abel, Laurent, Casanova, Jean-Laurent
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Sprache:eng
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