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

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