Different phenotypes of the same XIAP mutation in a family: A case of XIAP deficiency with juvenile idiopathic arthritis-Reference-Cited by-同舟云学术

Different phenotypes of the same XIAP mutation in a family: A case of XIAP deficiency with juvenile idiopathic arthritis

Author:

Shabani Mahsima¹²,Razaghian Anahita¹,Alimadadi Hosein³,Shiari Reza⁴,Shahrooei Mohammad⁵⁶,Parvaneh Nima¹²^ORCID

Affiliation:

1. Division of Allergy and Clinical Immunology, Department of PediatricsTehran University of Medical Sciences Tehran Iran

2. Research Center for ImmunodeficienciesTehran University of Medical Sciences Tehran Iran

3. Department of Pediatric Gastroeneterology, Children's Medical CenterTehran University of Medical Sciences Tehran Iran

4. Department of Pediatric Rheumatology, Mofid Children HospitalShahid Beheshti University of Medical Sciences Tehran Iran

5. Department of Microbiology and ImmunologyLaboratory of Clinical Bacteriology and Mycology, KU Leuven Leuven Belgium

6. Specialized Immunology Laboratory Ahvaz Iran

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

Reference14 articles.

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献