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Article

A Japanese family case with juvenile onset Behçet's disease caused by TNFAIP3 mutation.

Allergology international : official journal of the Japanese Society of Allergology - 1 Jan 2017

Ohnishi Hidenori, Kawamoto Norio, Seishima Mariko, Ohara Osamu, Fukao Toshiyuki

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 27451268
DOI: 10.1016/j.alit.2016.06.006

Genes

TNFAIP3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

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Research trail→

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A Japanese family case with juvenile onset Behçet's disease caused by TNFAIP3 mutation.PMID 27451268Read ↗

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Clinical and Genetic Aspects of Behçet's Disease in JapanSemantic proximity Read ↗

Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet’s diseaseSemantic proximity Read ↗

TNFAIP3 gene polymorphisms confer risk for Behcet's disease in a Chinese Han population.Semantic proximity Read ↗

TNF and TNF receptor polymorphisms in Korean Behcet’s disease patientsSemantic proximity Read ↗

The genetics of Behçet's disease in a Chinese population.Semantic proximity Read ↗

Three Chinese pedigrees of A20 haploinsufficiency: clinical, cytokine and molecular characterization.Semantic proximity Read ↗

Association of a TNIP1 polymorphism with Vogt-Koyanagi-Harada syndrome but not with ocular Behcet's disease in Han Chinese.Semantic proximity Read ↗

Autosomal dominant Hashimoto’s thyroiditis with a mutation in TNFAIP3Semantic proximity Read ↗

TRAF5 and TRAF3IP2 gene polymorphisms are associated with Behçet's disease and Vogt-Koyanagi-Harada syndrome: a case-control study.Semantic proximity Read ↗

Genetic Diagnosis and Identification of a Novel De Novo RELA Variant in Familial Behçet-like Autoinflammatory Syndrome Type 3: A Case Report.Semantic proximity Read ↗

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

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