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dc.contributor.authorYildirim, Erkan
dc.contributor.authorCelik, Guner
dc.contributor.authorYurdakul, Huseyin
dc.date.accessioned2019-06-06T09:50:44Z
dc.date.available2019-06-06T09:50:44Z
dc.date.issued2017
dc.identifier.issn1300-0667
dc.identifier.urihttp://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC5630112&blobtype=pdf
dc.identifier.urihttp://hdl.handle.net/11727/3407
dc.language.isoengen_US
dc.relation.isversionof10.5152/npa.2016.16997en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectPATENT FORAMEN OVALEen_US
dc.subjectFACTOR-V-LEIDENen_US
dc.subjectHEREDITARY HEMORRHAGIC TELANGIECTASIAen_US
dc.subjectPROTHROMBIN G20210A MUTATIONen_US
dc.subjectCEREBRAL-ISCHEMIAen_US
dc.subjectSTROKEen_US
dc.subjectTHROMBOPHILIAen_US
dc.subjectDEFICIENCYen_US
dc.subjectDELETIONen_US
dc.subjectADULTSen_US
dc.titleCerebrovascular Events Secondary to Pulmonary Arteriovenous Malformation Based on Genetic Heterogeneityen_US
dc.typeletteren_US
dc.relation.journalNOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRYen_US
dc.identifier.volume54en_US
dc.identifier.issue3en_US
dc.identifier.startpage286en_US
dc.identifier.endpage287en_US
dc.identifier.wos000412669100019


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