Associated Papers
A Case-Based Literature Review of RELA Associated Inflammatory Diseases.
Karaçayır N et al.
Journal of Clinical Immunology, 2026
RELA Haploinsufficiency Manifesting as an Atypical Phenotype of Crohn's Disease.
Tal N et al.
Inflammatory Bowel Diseases, 2025
Case report and literature review: clinical manifestations and treatment of human RelA deficiency.
Wang C et al.
Frontiers in Immunology, 2025
40134438 (PubMed )
Supplement: Table1.docx
Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity.
Moriya K et al.
The Journal of Experimental Medicine, 2023
Case report: Novel variants in RELA associated with familial Behcet's-like disease.
An JW et al.
Frontiers in Immunology, 2023
A Novel RELA Truncating Mutation in a Familial Behçet's Disease-like Mucocutaneous Ulcerative Condition.
Adeeb F et al.
Arthritis & Rheumatology (hoboken, N.j.), 2021
Primary Immunodeficiency Disease Mimicking Pediatric Bechet's Disease.
Shiraki M et al.
Children (basel, Switzerland), 2021
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