A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein
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Publication date
2015-09-28
Authors
Zhou, Q.
Wang, H.
Chae, J.
Yang, D.
Demirkaya, E.
Stoffels, M.
Takeuchi, M.
Chen, C.
Ombrello, A.
Schwartz, D.
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Article
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Abstract
Keywords
Rheumatology, Immunology and Allergy, Pediatrics, Perinatology, and Child Health
Citation
Zhou, Q, Wang, H, Chae, J, Yang, D, Demirkaya, E, Stoffels, M, Takeuchi, M, Chen, C, Ombrello, A, Schwartz, D, Hoffmann, P, Stone, D, Laxer, R, Royen-Kerkhof, A V, Ozen, S, Gadina, M, Kastner, D & Aksentijevich, I 2015, 'A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein', Pediatric Rheumatology, vol. 13, no. Suppl. 1, O71. https://doi.org/10.1186/1546-0096-13-S1-O71