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A Dominantly-Inherited Behcet-Like Disorder Caused By Haploinsufficiency Of The Tnfaip3/A20 Protein

dc.contributor.authorZhou, Q
dc.contributor.authorWang, H
dc.contributor.authorChae, J
dc.contributor.authorYang, D
dc.contributor.authorDemirkaya, E
dc.contributor.authorStoffels, M
dc.contributor.authorTakeuchi, M
dc.contributor.authorChen, C
dc.contributor.authorOmbrello, A
dc.contributor.authorSchwartz, D
dc.contributor.authorHoffmann, P
dc.contributor.authorStone, D
dc.contributor.authorLaxer, R
dc.contributor.authorRoyen-Kerkhof, AV
dc.contributor.authorOzen, Seza
dc.contributor.authorGadina, M
dc.contributor.authorKastner, D
dc.contributor.authorAksentijevich, I
dc.date.accessioned2019-12-10T10:42:09Z
dc.date.available2019-12-10T10:42:09Z
dc.date.issued2015
dc.identifier.issn1546-0096
dc.identifier.urihttps://doi.org/10.1186/1546-0096-13-S1-O71
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4597176/
dc.identifier.urihttp://hdl.handle.net/11655/14218
dc.relation.isversionof10.1186/1546-0096-13-S1-O71
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleA Dominantly-Inherited Behcet-Like Disorder Caused By Haploinsufficiency Of The Tnfaip3/A20 Protein
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalPediatric Rheumatology Online Journal
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları
dc.identifier.volume13
dc.identifier.issueSuppl 1
dc.identifier.startpageO71
dc.description.indexPubMed
dc.description.indexScopus


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