A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein. Issue 1 (December 2015)

Record Type:: Journal Article
Title:: A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein. Issue 1 (December 2015)
Main Title:: A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein
Authors:: 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
Abstract:
Is Part Of:: Pediatric rheumatology online journal. Volume 13:Issue 1(2015)
Journal:: Pediatric rheumatology online journal
Issue:: Volume 13:Issue 1(2015)
Issue Display:: Volume 13, Issue 1 (2015)
Year:: 2015
Volume:: 13
Issue:: 1
Issue Sort Value:: 2015-0013-0001-0000
Page Start:: 1
Page End:: 2
Publication Date:: 2015-12
Subjects:: Pediatric rheumatology -- Periodicals
Rheumatism in children -- Periodicals
618.92723
Journal URLs:: http://www.ped-rheum.com ↗
http://www.pedrheumonlinejournal.org ↗
http://link.springer.com/ ↗
DOI:: 10.1186/1546-0096-13-S1-O71 ↗
Languages:: English
ISSNs:: 1546-0096
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 10026.xml