Double Trouble: Novel Digenic CD19-RABEP2 Deletion in Predominantly Antibody Deficiency with Syndromic Features
Author:
Funder
Indian Council of Medical Research
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s10875-024-01745-2.pdf
Reference6 articles.
1. Wentink MWJ, van Zelm MC, van Dongen JJM, Warnatz K, van der Burg M. Deficiencies in the CD19 complex. Clin Immunol. 2018;195:82–7. https://doi.org/10.1016/j.clim.2018.07.017.
2. van Zelm MC, Reisli I. CD19 Deficiency due to Genetic Defects in the CD19 and CD81 Genes. In: D’Elios MM, Rizzi M, editors. Rare Diseases of the Immune System. Cham: Springer International Publishing; 2019. pp. 83–95. https://doi.org/10.1007/978-3-319-91785-6_7.
3. Deenick EK, Lau A, Bier J, Kane A. Molecular and cellular mechanisms underlying defective antibody responses. Immunol Cell Biol. 2020;98(6):467–79.
4. Küççüktürk S, Karaselek MA, Duran T, Reisli İ. Evaluation of transcription factors and cytokine expressions of T-cell subsets in CD19 deficiency and their possible relationship with autoimmune disease. Apmis. 2024;132(2):122–9.
5. Kofler N, Corti F, Rivera-Molina F, Deng Y, Toomre D, Simons M. The rab-effector protein RABEP2 regulates endosomal trafficking to mediate vascular endothelial growth factor receptor-2 (VEGFR2)-dependent signaling. J Biol Chem. 2018;293(13):4805–17.
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