Deleterious variants in TNFAIP3 are associated with type II and seronegative pediatric autoimmune hepatitis
Author:
Funder
Cincinnati Children's Hospital Medical Center
Publisher
Elsevier BV
Subject
Hepatology
Reference7 articles.
1. Failure to regulate TNF-induced NF-kappaB and cell death responses in A20-deficient mice;Lee;Science,2000
2. Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease;Zhou;Nat Genet,2016
3. TNFAIP3 gene polymorphisms in three common autoimmune diseases: systemic lupus erythematosus, rheumatoid arthritis, and primary sjogren syndrome-association with disease susceptibility and clinical phenotypes in Italian patients;Ciccacci;J Immunol Res,2019
4. Clinical spectrum and genetic causes of mitochondrial hepatopathy phenotype in children;Squires;Hepatol Commun,2023
5. Development of a validated interferon score using NanoString technology;Kim;J Interferon Cytokine Res,2018
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