Associated Papers
Novel loss-of-function intronic mutation in ELF4 is associated with intestinal autoinflammation.
Tian C et al.
Mucosal Immunology, 2025
Two novel frameshift variations in the ELF4 gene expand the mutational spectrum of DEX: case report and literature review.
Sun M et al.
Translational Pediatrics, 2025
40800195 (PubMed )
Supplement: tp-14-07-1675-supplementary.pdf
Current understanding of ELF4 deficiency: a novel inborn error of immunity.
Du HQ et al.
World Journal of Pediatrics : Wjp, 2024
"Deficiency in ELF4, X-Linked": a Monogenic Disease Entity Resembling Behçet's Syndrome and Inflammatory Bowel Disease.
Olyha SJ et al.
Journal of Clinical Immunology, 2024
A Multicenter Cohort Study of Immune Dysregulation Disorders Caused by ELF4 Variants in China.
Sun G et al.
Journal of Clinical Immunology, 2023
Loss of Function Mutation in ELF4 Causes Autoinflammatory and Immunodeficiency Disease in Human.
Sun G et al.
Journal of Clinical Immunology, 2022
Human autoinflammatory disease reveals ELF4 as a transcriptional regulator of inflammation.
Tyler PM et al.
Nature Immunology, 2021
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