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Prevalence of factor V Leiden in patients with retinal vein occlusion

dc.contributor.authorSIRMA, Serkan Önder
dc.contributor.authorAKARCAY, Koray
dc.contributor.authorUnaltuna, Nihan
dc.contributor.authorOZBEK, UĞUR
dc.contributor.authorONGOR, Ercan
dc.contributor.authorGUNEY, Dilvin Berrak
dc.contributor.authorDEMIRCI, FYK
dc.contributor.authorKIR, N
dc.date.accessioned2021-03-05T17:36:18Z
dc.date.available2021-03-05T17:36:18Z
dc.date.issued1999
dc.identifier.citationDEMIRCI F., GUNEY D. B. , AKARCAY K., KIR N., OZBEK U., SIRMA S. Ö. , Unaltuna N., ONGOR E., "Prevalence of factor V Leiden in patients with retinal vein occlusion", ACTA OPHTHALMOLOGICA SCANDINAVICA, cilt.77, sa.6, ss.631-633, 1999
dc.identifier.issn1395-3907
dc.identifier.othervv_1032021
dc.identifier.otherav_c65b3505-93a8-44bb-8822-f745ed1be2b9
dc.identifier.urihttp://hdl.handle.net/20.500.12627/131506
dc.description.abstractPurpose: Factor V Leiden mutation is a common genetic defect associated with a tendency to venous thrombosis. The aim of this study was to evaluate the prevalence of factor V Leiden in patients with retinal vein occlusion (RVO),
dc.language.isoeng
dc.subjectTıp
dc.subjectGöz Hastalıkları ve Cerrahisi
dc.subjectSağlık Bilimleri
dc.subjectCerrahi Tıp Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectOFTALMOLOJİ
dc.titlePrevalence of factor V Leiden in patients with retinal vein occlusion
dc.typeMakale
dc.relation.journalACTA OPHTHALMOLOGICA SCANDINAVICA
dc.contributor.department, ,
dc.identifier.volume77
dc.identifier.issue6
dc.identifier.startpage631
dc.identifier.endpage633
dc.contributor.firstauthorID28690


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