Associated Papers
Haploinsufficiency of A20 in a Chinese child caused by loss-of-function mutations in TNFAIP3: A case report and review of the literature.
Liu J et al.
Frontiers in Pediatrics, 2022
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 )
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