No Overt Clinical Immunodeficiency Despite Immune Biological Abnormalities in Patients With Constitutional Mismatch Repair Deficiency

Tesch, V.K.; IJspeert, H.; Raicht, A.; Rueda, D.; Dominguez-Pinilla, N.; Allende, L.M.; ... ; Seidel, M.G. (2018)

Article / Letter to editor

• primary immunodeficiency
• hyper-IgM syndrome
• DNA repair defect
• mismatch repair
• somatic hypermutation
• class-switch recombination
• IgA deficiency
• IgG subclass deficiency

• All authors: Tesch, V.K.; IJspeert, H.; Raicht, A.; Rueda, D.; Dominguez-Pinilla, N.; Allende, L.M.; Colas, C.; Rosenbaum, T.; Ilencikova, D.; Baris, H.N.; Nathrath, M.H.M.; Suerink, M.; Januszkiewicz-Lewandowska, D.; Ragab, I.; Azizi, A.A.; Wenzel, S.S.; Zschocke, J.; Schwinger, W.; Kloor, M.; Blattmann, C.; Brugieres, L.; Burg, M. van der; Wimmer, K.; Seidel, M.G.
• Date: 2018-07-02
• Journal: Frontiers in Immunology
• Volume: 9
• DOI: doi:10.3389/fimmu.2018.01506
• Link: https://www.frontiersin.org/articles/10.3389/fimmu.2018.01506/full