Lymphocyte Apoptosis and FAS Expression in Patients with 22q11.2 Deletion Syndrome
Author:
Funder
The South-Eastern Norway Regional Health Authority
Publisher
Springer Science and Business Media LLC
Subject
Immunology,Immunology and Allergy
Link
http://link.springer.com/article/10.1007/s10875-018-0579-7/fulltext.html
Reference34 articles.
1. McDonald-McGinn DM, Sullivan KE, Marino B, Philip N, Swillen A, Vorstman JA, et al. 22q11.2 deletion syndrome. Nat Rev Dis Primers. 2015;1:15071. https://doi.org/10.1038/nrdp.2015.71 .
2. Oskarsdottir S, Vujic M, Fasth A. Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden. Arch Dis Child. 2004;89(2):148–51.
3. Lima K, Folling I, Eiklid KL, Natvig S, Abrahamsen TG. Age-dependent clinical problems in a Norwegian national survey of patients with the 22q11.2 deletion syndrome. Eur J Pediatr. 2010;169(8):983–9. https://doi.org/10.1007/s00431-010-1161-3 .
4. McDonald-McGinn DM, Sullivan KE. Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome). Medicine (Baltimore). 2011;90(1):1–18. https://doi.org/10.1097/MD.0b013e3182060469 .
5. Crowley B, Ruffner M, McDonald McGinn DM, Sullivan KE. Variable immune deficiency related to deletion size in chromosome 22q11.2 deletion syndrome. Am J Med Genet A. 2018. https://doi.org/10.1002/ajmg.a.38597 .
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Case report: Effectiveness of sirolimus in treating partial DiGeorge Syndrome with Autoimmune Lymphoproliferative Syndrome (ALPS)-like features;Frontiers in Pediatrics;2023-01-18
2. T Cell Transcriptome in Chromosome 22q11.2 Deletion Syndrome;The Journal of Immunology;2022-09-01
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