Punctate inner choroidopathy in common variable immunodeficiency associated with a pathogenic variant in the tumour necrosis factor receptor superfamily 13b (TNFRSF13B) gene - Case report and review of the literature

Punctate inner choroidopathy in common variable immunodeficiency associated with a pathogenic variant in the tumour necrosis factor receptor superfamily 13b (TNFRSF13B) gene - Case report and review of the literature

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Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 255(2023) vom: 20. Okt., Seite 109748
1. Verfasser: Salih, Hiba (VerfasserIn)
Weitere Verfasser: Wai, Kelvin Cheng Kah, McKee, Justin, Chopra, Charu
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2023
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Review Case Reports Journal Article Autoimmunity Common variable immunodeficiency Punctuate inner choroidopathy TNFRSF13B protein, human Transmembrane Activator and CAML Interactor Protein
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