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Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behcet's Disease

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dc.contributor.authorsOgnenovski, Mikhail; Renauer, Paul; Koetter, Ina; Henes, Joerg C.; Casali, Bruno; Salvarani, Carlo; Direskeneli, Haner; Kaufman, Kenneth M.; Sawalha, Amr H.
dc.date.accessioned2022-03-10T17:53:52Z
dc.date.accessioned2026-01-10T17:24:32Z
dc.date.available2022-03-10T17:53:52Z
dc.date.issued2015
dc.identifier.doidoiWOS:000370860204773
dc.identifier.eissn2326-5205
dc.identifier.issn2326-5191
dc.identifier.urihttps://hdl.handle.net/11424/221752
dc.identifier.wosWOS:000370860204773
dc.language.isoeng
dc.publisherWILEY-BLACKWELL
dc.relation.ispartofARTHRITIS & RHEUMATOLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleWhole Exome Sequencing Identifies Rare Protein-Coding Variants in Behcet's Disease
dc.typeconferenceObject
dc.type.submeetingabstract
dspace.entity.typePublication
oaire.citation.titleARTHRITIS & RHEUMATOLOGY
oaire.citation.volume67

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