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Paediatrics Publications

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

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 SciencesFollow
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)

Document Type

Article

Publication Date

9-28-2015

Journal

Pediatric Rheumatology

Volume

13

Issue

1

URL with Digital Object Identifier

10.1186/1546-0096-13-S1-O71

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