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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
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 |
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