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Selected Works of Erkan Demirkaya
Article
A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein
Pediatric Rheumatology
  • Q. Zhou, National Human Genome Research Institute (NHGRI)
  • H. Wang, National Human Genome Research Institute (NHGRI)
  • J. Chae, National Human Genome Research Institute (NHGRI)
  • D. Yang, National Institutes of Health (NIH)
  • E. Demirkaya, University of Medical Sciences
  • M. Stoffels, National Human Genome Research Institute (NHGRI)
  • M. Takeuchi, National Human Genome Research Institute (NHGRI)
  • C. Chen, National Human Genome Research Institute (NHGRI)
  • A. Ombrello, National Human Genome Research Institute (NHGRI)
  • D. Schwartz, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
  • P. Hoffmann, National Human Genome Research Institute (NHGRI)
  • D. Stone, National Human Genome Research Institute (NHGRI)
  • R. Laxer, Hospital for Sick Children University of Toronto
  • A. V. Royen-Kerkhof, University Medical Center Utrecht
  • S. Ozen, Hacettepe Üniversitesi
  • M. Gadina, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
  • D. Kastner, National Human Genome Research Institute (NHGRI)
  • I. Aksentijevich, National Human Genome Research Institute (NHGRI)
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Document Type
Article
Publication Date
9-28-2015
URL with Digital Object Identifier
10.1186/1546-0096-13-S1-O71
Citation Information
Q. Zhou, H. Wang, J. Chae, D. Yang, et al.. "A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein" Pediatric Rheumatology Vol. 13 Iss. 1 (2015)
Available at: http://works.bepress.com/erkan-demirkaya/11/