Conference
Limited genotype-phenotype correlation in FOXP3 gene within same family member
Abstract
Introduction: FOXP3 protein is crucial in enabling T-regulatory cells to maintain tolerance to self-antigens. Mutations in human Foxp3 gene are associated with immune diseases, such as multi-organ autoimmune disorder, immune dysregulation, polyendocrinopathy, enteropathy and X-linked syndrome (IPEX).
Authors
Sharaf M; Alaaraj N; Shurrab S; Zangen D
Name of conference
European Society of Pediatric Endocrinology.
Conference place
Rome, Italy.
Conference start date
September 15, 2022
Conference end date
September 17, 2022