Wang W, Wang J, Wang J, Liu J, Pei J, Li W, et al. Whole-exome sequencing identified a homozygous novel RAG1 mutation in a child with omenn syndrome. Allergol Immunopathol [Internet]. 2022 Nov. 1 [cited 2026 Jun. 24];50(6):32-46. Available from: https://www.all-imm.com/index.php/aei/article/view/529