Novel heterozygous C243Y A20/TNFAIP3 gene mutation is responsible for chronic inflammation in autosomal-dominant Behçet's disease-Reference-Cited by-同舟云学术

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Novel heterozygous C243Y A20/TNFAIP3 gene mutation is responsible for chronic inflammation in autosomal-dominant Behçet's disease

Published:2016-05 Issue:1 Volume:2 Page:e000223
ISSN:2056-5933
Container-title:RMD Open
language:en
Short-container-title:RMD Open

Author:

Shigemura Tomonari,Kaneko Naoe,Kobayashi Norimoto,Kobayashi Keiko,Takeuchi Yusuke,Nakano Naoko,Masumoto Junya,Agematsu Kazunaga

Publisher

BMJ

Subject

Immunology,Immunology and Allergy,Rheumatology

Cited by 78 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. Genetic Mutations Associated With TNFAIP3 (A20) Haploinsufficiency and Their Impact on Inflammatory Diseases;International Journal of Molecular Sciences;2024-07-29

2. A20 Haploinsufficiency: A Systematic Review of 177 Cases;Journal of Investigative Dermatology;2023-12

3. Uveitis Associated with Monogenic Autoinflammatory Syndromes in Children;Ocular Immunology and Inflammation;2023-11-26

4. Haploinsufficiency of A20 caused by a novel pathogenic missense variant of TNFAIP3 and successfully treated with anti-TNF and immunosuppressive therapies;Cellular Immunology;2023-09

5. A critical region of A20 unveiled by missense TNFAIP3 variations that lead to autoinflammation;eLife;2023-06-21

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