Associated Papers
Multicenter international cohort study of HA20 reveals novel genetic architecture and phenotypic evolution.
He T et al.
The Journal of Allergy and Clinical Immunology, 2026
Genetic Mutations Associated With TNFAIP3 (A20) Haploinsufficiency and Their Impact on Inflammatory Diseases.
Bagyinszky E et al.
International Journal of Molecular Sciences, 2024
Case report: Adult case of A20 haploinsufficiency suspected as neuro-Behçet disease.
Shirai H et al.
Frontiers in Immunology, 2024
Novel loss-of-function mutations in TNFAIP3 gene in patients with lupus nephritis.
Zhang C et al.
Clinical Kidney Journal, 2022
Mutation analysis of the TNFAIP3 in A20 haploinsufficiency: A case report.
Yan M et al.
Medicine, 2021
Haploinsufficiency of A20 (HA20): updates on the genetics, phenotype, pathogenesis and treatment.
Yu MP et al.
World Journal of Pediatrics : Wjp, 2020
Association of Clinical Phenotypes in Haploinsufficiency A20 (HA20) With Disrupted Domains of A20.
Chen Y et al.
Frontiers in Immunology, 2020
33101300 (PubMed )
Supplement: Data_Sheet_3.PDF
Novel Heterogeneous Mutation of TNFAIP3 in a Chinese Patient with Behçet-Like Phenotype and Persistent EBV Viremia.
Dong X et al.
Journal of Clinical Immunology, 2019
TNFAIP3 haploinsufficiency is the cause of autoinflammatory manifestations in a patient with a deletion of 13Mb on chromosome 6.
Franco-Jarava C et al.
Clinical Immunology (orlando, Fla.), 2018
An Update on Autoinflammatory Diseases: Relopathies.
Steiner A et al.
Current Rheumatology Reports, 2018
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease.
Zhou Q et al.
Nature Genetics, 2016
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