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

Q. Zhou; H. Wang; J. Chae; D. Yang; E. Demirkaya; M. Stoffels; M. Takeuchi; C. Chen; A. Ombrello; D. Schwartz; P. Hoffmann; D. Stone; R. Laxer; A. V. Royen-Kerkhof; S. Ozen; M. Gadina; D. Kastner; I. Aksentijevich

doi:10.1186/1546-0096-13-S1-O71

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

Q. Zhou
, H. Wang
, J. Chae
, D. Yang
, E. Demirkaya
, M. Stoffels
, M. Takeuchi
, C. Chen
, A. Ombrello
, D. Schwartz
, P. Hoffmann
, D. Stone
, R. Laxer
, A. V. Royen-Kerkhof
, S. Ozen
, M. Gadina
, D. Kastner
, I. Aksentijevich^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

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Original language	English
Article number	O71
Journal	Pediatric Rheumatology
Volume	13
Issue number	Suppl. 1
DOIs	https://doi.org/10.1186/1546-0096-13-S1-O71
Publication status	Published - 28 Sept 2015

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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, 13(Suppl. 1), Article O71. https://doi.org/10.1186/1546-0096-13-S1-O71

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

author = "Q. Zhou and H. Wang and J. Chae and D. Yang and E. Demirkaya and M. Stoffels and M. Takeuchi and C. Chen and A. Ombrello and D. Schwartz and P. Hoffmann and D. Stone and R. Laxer and Royen-Kerkhof, \{A. V.\} and S. Ozen and M. Gadina and D. Kastner and I. Aksentijevich",

note = "8th International Congress of Familial Mediterranean Fever and Systemic Autoinflammatory Diseases",

year = "2015",

month = sep,

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doi = "10.1186/1546-0096-13-S1-O71",

language = "English",

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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, AV, 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

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T1 - A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein

AU - Zhou, Q.

AU - Wang, H.

AU - Chae, J.

AU - Yang, D.

AU - Demirkaya, E.

AU - Stoffels, M.

AU - Takeuchi, M.

AU - Chen, C.

AU - Ombrello, A.

AU - Schwartz, D.

AU - Hoffmann, P.

AU - Stone, D.

AU - Laxer, R.

AU - Royen-Kerkhof, A. V.

AU - Ozen, S.

AU - Gadina, M.

AU - Kastner, D.

AU - Aksentijevich, I.

N1 - 8th International Congress of Familial Mediterranean Fever and Systemic Autoinflammatory Diseases

PY - 2015/9/28

Y1 - 2015/9/28

UR - https://www.scopus.com/pages/publications/84956791368

U2 - 10.1186/1546-0096-13-S1-O71

DO - 10.1186/1546-0096-13-S1-O71

M3 - Article

AN - SCOPUS:84956791368

SN - 1546-0096

VL - 13

JO - Pediatric Rheumatology

JF - Pediatric Rheumatology

IS - Suppl. 1

M1 - O71

ER -

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

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