Multi-omics analysis of naïve B cells of patients harboring the C104R mutation in TACI

Common variable immunodeficiency (CVID) is the most prevalent form of symptomatic primary immunodeficiency in humans. The genetic cause of CVID is still unknown in about 70% of cases. Ten percent of CVID patients carry heterozygous mutations in the tumor necrosis factor receptor superfamily member 1...

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Detalles Bibliográficos
Autores principales: Ramirez, Neftali, Posadas-Cantera, Sara, Langer, Niko, de Oteyza, Andres Caballero Garcia, Proietti, Michele, Keller, Baerbel, Zhao, Fangwen, Gernedl, Victoria, Pecoraro, Matteo, Eibel, Hermann, Warnatz, Klaus, Ballestar, Esteban, Geiger, Roger, Bossen, Claudia, Grimbacher, Bodo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443529/
https://www.ncbi.nlm.nih.gov/pubmed/36072607
http://dx.doi.org/10.3389/fimmu.2022.938240

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443529/
https://www.ncbi.nlm.nih.gov/pubmed/36072607
http://dx.doi.org/10.3389/fimmu.2022.938240

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