Case report and literature review: clinical manifestations and treatment of human RelA deficiency

RelA deficiency resulting from mutations in the human RELA gene is a recently identified inborn errors of immunity (IEI). The RELA gene encodes the RelA (p65) protein, one of the five transcription factors of the NF-κB family, which plays a critical role in the regulation of transcriptional programs...

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Autori principali:	Chenghao Wang, Wenjie Wang, Xiaoying Hui, Jia Hou, Qinhua Zhou, Qifan Li, Qi Wu, Qi Ni, Bingbing Wu, Jinqiao Sun, Xiaochuan Wang
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Frontiers Media S.A. 2025-02-01
Serie:	Frontiers in Immunology
Soggetti:	RelA deficiency NF-κB recurrent oral ulcers Behçet’s disease case report
Accesso online:	https://www.frontiersin.org/articles/10.3389/fimmu.2025.1529654/full
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