Budd-Chiari syndrome in a patient heterozygous for the point mutation C20221T of the prothrombin gene

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dc.contributor.authorBalim, Z
dc.contributor.authorKosova, B
dc.contributor.authorFalzon, K
dc.contributor.authorWettinger, SB
dc.contributor.authorColak, Y
dc.date.accessioned2019-10-27T18:40:12Z
dc.date.available2019-10-27T18:40:12Z
dc.date.issued2003
dc.departmentEge Üniversitesien_US
dc.identifier.doi10.1046/j.1538-7836.2003.t01-2-00115.xen_US
dc.identifier.endpage853en_US
dc.identifier.issn1538-7933
dc.identifier.issue4en_US
dc.identifier.pmid12871427en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage852en_US
dc.identifier.urihttps://doi.org/10.1046/j.1538-7836.2003.t01-2-00115.x
dc.identifier.urihttps://hdl.handle.net/11454/36878
dc.identifier.volume1en_US
dc.identifier.wosWOS:000183062100040en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherBlackwell Publ Ltden_US
dc.relation.ispartofJournal of Thrombosis and Haemostasisen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleBudd-Chiari syndrome in a patient heterozygous for the point mutation C20221T of the prothrombin geneen_US
dc.typeLetteren_US

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