Associated Papers
Genetic Mutations Associated With TNFAIP3 (A20) Haploinsufficiency and Their Impact on Inflammatory Diseases.
Bagyinszky E et al.
International Journal of Molecular Sciences, 2024
Autosomic dominant familial Behçet disease and haploinsufficiency A20: A review of the literature.
Berteau F et al.
Autoimmunity Reviews, 2018
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease.
Zhou Q et al.
Nature Genetics, 2016
Select a paper to view details