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

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.

doi:https://doi.org/10.1186/1546-0096-13-S1-O71

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

DSpace/Manakin Repository

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

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) Pediatric Rheumatology, volume 13, issue Suppl. 1

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Keywords: Rheumatology, Immunology and Allergy, Pediatrics, Perinatology, and Child Health

DOI: https://doi.org/10.1186/1546-0096-13-S1-O71

ISSN: 1546-0096

Publisher: BioMed Central

Note: 8th International Congress of Familial Mediterranean Fever and Systemic Autoinflammatory Diseases

(Peer reviewed)