Heterogeneity in RAG1 and RAG2 deficiency: 35 cases from a single-centre.

导出 OA

翻译打印收藏纠错

作者： Betul,Karaatmaca ^[1] ; Deniz,Cagdas ^[2] ; Saliha,Esenboga ^[1] ; Baran,Erman ^[3] ; Cagman,Tan ^[1] ; Tuba,Turul Ozgur ^[3] ; Kaan,Boztug ^[3] ; Mirjam,van der Burg ^[1] ; Ozden,Sanal ^[4] ; Ilhan,Tezcan ^[5]

作者单位： Hacettepe University School of Medicine, Department of Pediatrics, Division of Pediatric Immunology, Ankara, Turkey. ^[1] Department of Pediatric Allergy and Immunology, University of Health Sciences, Ankara Bilkent City Hospital, Ankara, Turkey. ^[2] Section of Pediatric Immunology, Institute of Child Health, Hacettepe University, Ankara, Turkey. ^[3] St. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria. ^[4] CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria. ^[5] Medical University of Vienna, Department of Pediatrics and Adolescent Medicine, Vienna, Austria. ^[6] Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria. ^[7] St. Anna Children's Hospital, Vienna, Austria. ^[8] Department of Pediatrics, Laboratory for Pediatric Immunology, Willem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, The Netherlands. ^[9]

关键词 Omenn syndrome RAG1/2 autoimmunity erythroderma severe combined immunodeficiency vasculitis