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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Détails bibliographiques
| Publié dans: | Clinical immunology (Orlando, Fla.). - 1999. - 255(2023) vom: 20. Okt., Seite 109748
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| Auteur principal: |
Salih, Hiba
(Auteur) |
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| Autres auteurs: |
Wai, Kelvin Cheng Kah,
McKee, Justin,
Chopra, Charu |
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| Format: | Article en ligne
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| Langue: | English |
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| Publié: |
2023
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| Accès à la collection: | Clinical immunology (Orlando, Fla.)
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| Sujets: | 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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