Recombinant IFN-γ1b Treatment in a Patient with Inherited IFN-γ Deficiency

Recombinant IFN-γ1b Treatment in a Patient with Inherited IFN-γ Deficiency

<h3>Purpose</h3><p dir="ltr">Inborn errors of IFN-γ immunity underlie Mendelian susceptibility to mycobacterial disease (MSMD). Twenty-two genes with products involved in the production of, or response to, IFN-γ and variants of which underlie MSMD have been identified. Ho...

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محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: Jérémie Rosain (5900399) (author)
مؤلفون آخرون: Ayca Kiykim (13851559) (author), Alexandre Michev (19342507) (author), Yasemin Kendir-Demirkol (19342510) (author), Darawan Rinchai (742366) (author), Jessica N. Peel (19342513) (author), Hailun Li (14896062) (author), Suheyla Ocak (11158408) (author), Pinar Gokmirza Ozdemir (19342516) (author), Tom Le Voyer (18551572) (author), Quentin Philippot (558140) (author), Taushif Khan (691254) (author), Anna-Lena Neehus (9320912) (author), Mélanie Migaud (5913107) (author), Camille Soudée (19342519) (author), Stéphanie Boisson-Dupuis (64693) (author), Nico Marr (349853) (author), Alessandro Borghesi (1871344) (author), Jean-Laurent Casanova (64712) (author), Jacinta Bustamante (64702) (author)
منشور في: 2024
الموضوعات:
Biological sciences
Genetics
Biomedical and clinical sciences
Clinical sciences
Immunology
Inborn error of immunity
Interferon-gamma
Mycobacterium
BCG
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