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A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein

Authors
  • Zhou, Q1
  • Wang, H1
  • Chae, J1
  • Yang, D2
  • Demirkaya, E3
  • Stoffels, M1
  • Takeuchi, M1
  • Chen, C1
  • Ombrello, A1
  • Schwartz, D4
  • Hoffmann, P1
  • Stone, D1
  • Laxer, R5
  • Royen-Kerkhof, AV6
  • Ozen, S7
  • Gadina, M4
  • Kastner, D1
  • Aksentijevich, I1
  • 1 NHGRI/NIH, Bethesda, USA , Bethesda (United States)
  • 2 NHLBI/NIH, Bethesda, USA , Bethesda (United States)
  • 3 Institute of Health Sciences, Ankara, Turkey , Ankara (Turkey)
  • 4 NIAMS/NIH, Bethesda, USA , Bethesda (United States)
  • 5 The Hospital for Sick Children, Toronto, Canada , Toronto (Canada)
  • 6 Universitair Medisch Centrum Utrecht, Utrecht, Netherlands , Utrecht (Netherlands)
  • 7 Hacettepe University, Ankara, Turkey , Ankara (Turkey)
Type
Published Article
Journal
Pediatric Rheumatology
Publisher
Springer Science and Business Media LLC
Publication Date
Sep 28, 2015
Volume
13
Issue
Suppl 1
Identifiers
DOI: 10.1186/1546-0096-13-S1-O71
Source
Springer Nature
Keywords
License
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