Associated Papers
Three Chinese pedigrees of A20 haploinsufficiency: clinical, cytokine and molecular characterization.
Tian Y et al.
Frontiers in Immunology, 2022
Mutation analysis of the TNFAIP3 in A20 haploinsufficiency: A case report.
Yan M et al.
Medicine, 2021
A20 at the Crossroads of Cell Death, Inflammation, and Autoimmunity.
Martens A et al.
Cold Spring Harbor Perspectives in Biology, 2020
Autosomic dominant familial Behçet disease and haploinsufficiency A20: A review of the literature.
Berteau F et al.
Autoimmunity Reviews, 2018
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
A Japanese family case with juvenile onset Behçet's disease caused by TNFAIP3 mutation.
Ohnishi H et al.
Allergology International : Official Journal of the Japanese Society of Allergology, 2017
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