1. A case report of novel mutation in PRF1 gene, which causes familial autosomal recessive hemophagocytic lymphohistiocytosis
   Mohammad Reza Bordbar et al, 2017, BMC Medical Genetics CrossRef
2. Novel X-Linked Inhibitor of Apoptosis Mutation in Very Early-Onset Inflammatory Bowel Disease Child Successfully Treated with HLA-Haploidentical Hemapoietic Stem Cells Transplant after Removal of αβ+ T and B Cells
   Cristina Cifaldi et al, 2017, Frontiers in Immunology CrossRef
3. X-linked lymphoproliferative syndrome in mainland China: review of clinical, genetic, and immunological characteristic
   Tao Xu et al, 2020, European Journal of Pediatrics CrossRef
4. Haploidentical Hematopoietic Stem Cell Transplantation for XIAP Deficiency: a Single-Center Report
   Jun Yang et al, 2020, Journal of Clinical Immunology CrossRef
5. Evolution of Our Understanding of XIAP Deficiency
   Anne C. A. Mudde et al, 2021, Frontiers in Pediatrics CrossRef
6. Nucleotide-binding oligomerization domain (NOD) signaling defects and cell death susceptibility cannot be uncoupled in X-linked inhibitor of apoptosis (XIAP)-driven inflammatory disease
   Steven M. Chirieleison et al, 2017, Journal of Biological Chemistry CrossRef
7. HLH as an additional warning sign of inborn errors of immunity beyond familial-HLH in children: a systematic review
   Silvia Ricci et al, 2024, Frontiers in Immunology CrossRef
8. Phenotype, genotype, treatment, and survival outcomes in patients with X-linked inhibitor of apoptosis deficiency
   Linlin Yang et al, 2022, Journal of Allergy and Clinical Immunology CrossRef