Novel Mutation of ZAP-70-related Combined Immunodeficiency: First Case from the National Iranian Registry and Review of the Literature-Reference-Cited by-同舟云学术

Novel Mutation of ZAP-70-related Combined Immunodeficiency: First Case from the National Iranian Registry and Review of the Literature

Published:2016-10-19 Issue:1 Volume:46 Page:70-79
ISSN:0882-0139
Container-title:Immunological Investigations
language:en
Short-container-title:Immunological Investigations

Author:

Shirkani Afshin,Shahrooei Mohammad,Azizi Gholamreza,Rokni-Zadeh Hassan,Abolhassani Hassan,Farrokhi Shokrollah,Frans Glynis,Bossuyt Xavier,Aghamohammadi Asghar

Publisher

Informa UK Limited

Subject

General Medicine,Immunology

Link

http://www.tandfonline.com/doi/pdf/10.1080/08820139.2016.1214962

Reference40 articles.

1. A hypomorphic recombination-activating gene 1 (RAG1) mutation resulting in a phenotype resembling common variable immunodeficiency

2. Primary Immunodeficiency Disorders in Iran: Update and New Insights from the Third Report of the National Registry

3. Silent brain infarcts in two patients with zeta chain-associated protein 70kDa (ZAP70) deficiency

4. Defective T cell receptor signaling and CD8+ thymic selection in humans lacking Zap-70 kinase

Cited by 21 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. Regulating the discriminatory response to antigen by T-cell receptor;Bioscience Reports;2022-03

2. A novel zeta-associated protein 70 homozygous mutation causing combined immunodeficiency presenting as neonatal autoimmune hemolytic anemia;Immunologic Research;2021-01-23

3. Letter from the Editor 2020: Annual Summary and Introduction of the Thematic Issue and Guest Editor;Immunological Investigations;2020-10-02

4. A novel hypomorphic ζ-chain-associated protein tyrosine kinase 70 kDa mutation with normal CD8+ T cells count;Chinese Medical Journal;2020-07-01

5. Clinical, Immunological, and Genetic Features in 49 Patients With ZAP-70 Deficiency: A Systematic Review;Frontiers in Immunology;2020-05-05