Associated Papers
Pitfalls in the diagnosis of apparent homozygous mutations: two cases of IL10RA deficiency inflammatory bowel disease and a literature review.
Shi X et al.
Orphanet Journal of Rare Diseases, 2025
Case Report: A Novel Compound Heterozygous Mutation in IL-10RA in a Chinese Child With Very Early-Onset Inflammatory Bowel Disease.
Dong F et al.
Frontiers in Pediatrics, 2021
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