WANG, Wendi et al. Whole-exome sequencing identified a homozygous novel RAG1 mutation in a child with omenn syndrome. Allergologia et Immunopathologia, Singapore, v. 50, n. 6, p. 32–46, 2022. DOI: 10.15586/aei.v50i6.529. Disponível em: https://www.all-imm.com/index.php/aei/article/view/529.. Acesso em: 24 jun. 2026.