1. Lopez-Herrera G, Tampella G, Baronio M, Vitali M, Lougaris V, Plebani A, et al. Mutations in LRBA are Associated with a Syndrome of Immune Deficiency and Autoimmunity. Journal of Clinical Immunology. 2012;32(2):363-4. 2. Gámez-Díaz L, August D, Stepensky P, Revel-Vilk S, Seidel MG, Noriko M, et al. The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency. Journal of Allergy and Clinical Immunology. 2016;137(1):223-30. 3. Serwas NK, Kansu A, Santos-Valente E, Kuloglu Z, Demir A, Yaman A, et al. Atypical manifestation of LRBA deficiency with predominant IBD-like phenotype. Inflammatory bowel diseases. 2015;21(1):40-7. 4. Alkhairy OK, Abolhassani H, Rezaei N, Fang M, Andersen KK, Chavoshzadeh Z, et al. Spectrum of phenotypes associated with mutations in LRBA. Journal of clinical immunology. 2016;36(1):33-45. 5. Alangari A, Alsultan A, Adly N, Massaad MJ, Kiani IS, Aljebreen A, et al. LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency. Journal of Allergy and Clinical Immunology. 2012;130(2):481-8. e2. 6. Lopez-Herrera G, Tampella G, PanHammarström Q, Herholz P, Trujillo-Vargas CM, Phadwal K, et al. Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. The American Journal of Human Genetics. 2012;90(6):986- 1001. 7. Azizi G, Ziaee V, Tavakol M, Alinia T,Yazdai R, Mohammadi H, et al. Approach to the Management of Autoimmunity in Primary Immunodeficiency. Scandinavian journal of immunology. 2017;85(1):13-29. 8. Tegtmeyer D, Seidl M, Gerner P, Baumann U, Klemann C. IBD due to PID: Inflammatory bowel disease caused by primary immunodeficiencies‐Clinical presentations, review of literature, and proposal of a rational diagnostic algorithm. Pediatric Allergy and Immunology. 2017. 9. Bratanič N, Kovač J, Pohar K, Podkrajšek KT, Ihan A, Battelino T, et al. Multifocal gastric adenocarcinoma in a patient with LRBA deficiency. Orphanet journal of rare diseases. 2017;12(1):131. 10. Agarwal S, Mayer L. Diagnosis and treatment of gastrointestinal disorders in patients with primary immunodeficiency. Clinical gastroenterology and hepatology. 2013;11(9):1050-63. 11. Aghamohammadi A, Mohammadinejad P, Abolhassani H, Mirminachi B, Movahedi M, Gharagozlou M, et al. Primary immunodeficiency disorders in Iran: update and new insights from the third report of the national registry. Journal of clinical immunology. 2014;34(4):478-90. 12. Conley ME, Notarangelo LD, Etzioni A. Diagnostic criteria for primary immunodeficiencies. Clinical immunology. 1999;93(3):190-7. 13. Arandi N, Mirshafiey A, Abolhassani H, Jeddi‐Tehrani M, Edalat R, Sadeghi B, et al. Frequency and expression of inhibitory markers of CD4+ CD25+ FOXP3+ regulatory T cells in patients with common variable immunodeficiency. Scandinavian journal of immunology. 2013;77(5):405-12. 14. Yazdani R, Seify R, Ganjalikhani-Hakemi M, Abolhassani H, Eskandari N, Golsaz-Shirazi F, et al. Comparison of various classifications for patients with common variable immunodeficiency (CVID) using measurement of B-cell subsets. Allergologia et immunopathologia. 2017;45(2):183-92. 15. Burns SO, Zenner HL, Plagnol V, Curtis J, Mok K, Eisenhut M, et al. LRBA gene deletion in a patient presenting with autoimmunity without hypogammaglobulinemia. The Journal of allergy and clinical immunology. 2012;130(6):1428. 16. Azizi G, Ahmadi M, Abolhassani H, Yazdani R, Mohammadi H, Mirshafiey A, et al. Autoimmunity in Primary Antibody Deficiencies. International archives of allergy and immunology. 2016;171(3-4):180-93. 17. Azizi G, Abolhassani H, Mahdaviani SA, Chavoshzadeh Z, Eshghi P, Yazdani R, et al. Clinical, Immunological, Molecular Analyses and Outcomes of Iranian Patients with LRBA Deficiency: A Longitudinal Study. Pediatric Allergy and Immunology. 2017. 18. Bal SK, Haskologlu S, Serwas NK, Islamoglu C, Aytekin C, Kendirli T, et al. Multiple Presentations of LRBA Deficiency: a Single-Center Experience. Journal of clinical immunology. 2017;37(8):790-800.19. Alangari A, Alsultan A, Adly N, Massaad MJ, Kiani IS, Aljebreen A, et al. LPS -responsive beige -like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency. The Journal of allergy and clinical immunology. 2012;130(2):481 -8.e2. 20. Uhlig HH. Monogenic diseases associated with intestinal inflammation: implications for the understanding of inflammatory bowel disease. Gut. 2013;62(12):1795 -805.