Hidradenitis suppurativa and Mediterranean fever gene mutations

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dc.authorscopusid55964991700
dc.authorscopusid57189506487
dc.authorscopusid57193691709
dc.authorscopusid57209528732
dc.contributor.authorİlgen U.
dc.contributor.authorYayla M.E.
dc.contributor.authorEyüpoğlu Ş.
dc.contributor.authorKarahan İ.
dc.date.accessioned2024-06-12T10:25:02Z
dc.date.available2024-06-12T10:25:02Z
dc.date.issued2019
dc.description.abstract[No abstract available]en_US
dc.identifier.doi10.1016/j.jdcr.2019.06.035
dc.identifier.endpage793en_US
dc.identifier.issn2352-5126
dc.identifier.issue9en_US
dc.identifier.scopus2-s2.0-85071398705en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage792en_US
dc.identifier.urihttps://doi.org/10.1016/j.jdcr.2019.06.035
dc.identifier.urihttps://hdl.handle.net/20.500.14551/16163
dc.identifier.volume5en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherElsevier Incen_US
dc.relation.ispartofJAAD Case Reportsen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAmyloid A Protein; Pyrin; Serum Amyloid A; Aa Amyloidosis; Behcet Disease; Disease Severity; Familial Mediterranean Fever; Gene Mutation; Heterozygote; Human; Inflammatory Bowel Disease; Inflammatory Disease; Letter; Molecular Pathology; Multiple Sclerosis; Priority Journal; Prognosis; Pyoderma Gangrenosum; Rheumatoid Arthritis; Spondyloarthropathy; Suppurative Hidradenitis; Vasculitisen_US
dc.titleHidradenitis suppurativa and Mediterranean fever gene mutationsen_US
dc.typeLetteren_US

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