Rare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from Canakkale

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dc.authoridSılan, Coşkun/0000-0002-8352-6571
dc.contributor.authorSılan, Fatma
dc.contributor.authorDjurovic, Jelena
dc.contributor.authorBir, Firdevs Dincsoy
dc.contributor.authorSılan, Coşkun
dc.contributor.authorÖzdemir, Öztürk
dc.date.accessioned2025-01-27T21:07:33Z
dc.date.available2025-01-27T21:07:33Z
dc.date.issued2018
dc.departmentÇanakkale Onsekiz Mart Üniversitesi
dc.descriptionEuropean Biotechnology Congress -- APR 26-28, 2018 -- Athens, GREECE
dc.description.abstract[Anstract Not Available]
dc.identifier.doi10.1016/j.jbiotec.2018.06.213
dc.identifier.endpageS65
dc.identifier.issn0168-1656
dc.identifier.issn1873-4863
dc.identifier.startpageS65
dc.identifier.urihttps://doi.org/10.1016/j.jbiotec.2018.06.213
dc.identifier.urihttps://hdl.handle.net/20.500.12428/28102
dc.identifier.volume280
dc.identifier.wosWOS:000454825900210
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.language.isoen
dc.publisherElsevier Science Bv
dc.relation.ispartofJournal of Biotechnology
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20250125
dc.titleRare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from Canakkale
dc.typeConference Object

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