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Mutations in the NOD2 gene are associated with a specific phenotype and lower anti-tumor necrosis factor trough levels in Crohn's disease

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dc.bibliographiccitation.firstpage678
dc.bibliographiccitation.issue11
dc.bibliographiccitation.journalJournal of Digestive Diseases
dc.bibliographiccitation.lastpage684
dc.bibliographiccitation.volume19
dc.contributor.authorSchäffler, Holger
dc.contributor.authorGeiss, David
dc.contributor.authorGittel, Nicole
dc.contributor.authorRohde, Sarah
dc.contributor.authorHuth, Astrid
dc.contributor.authorGlass, Änne
dc.contributor.authorBrandhorst, Gunnar
dc.contributor.authorJaster, Robert
dc.contributor.authorLamprecht, Georg
dc.date.accessioned2020-12-10T18:26:37Z
dc.date.available2020-12-10T18:26:37Z
dc.date.issued2018
dc.identifier.doi10.1111/1751-2980.12677
dc.identifier.eissn1751-2980
dc.identifier.issn1751-2972
dc.identifier.urihttps://resolver.sub.uni-goettingen.de/purl?gro-2/76139
dc.language.isoen
dc.notes.internDOI Import GROB-354
dc.titleMutations in the NOD2 gene are associated with a specific phenotype and lower anti-tumor necrosis factor trough levels in Crohn's disease
dc.typejournal_article
dc.type.internalPublicationyes
dspace.entity.typePublication

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