Prothrombin C20209T mutation in deep vein thrombosis: A case report

dc.creatorMuñoz M.
dc.creatorVilos C.
dc.creatorCantín M.
dc.date.accessioned2020-09-02T22:24:05Z
dc.date.accessioned2022-11-08T20:18:28Z
dc.date.available2020-09-02T22:24:05Z
dc.date.available2022-11-08T20:18:28Z
dc.date.created2020-09-02T22:24:05Z
dc.date.issued2015
dc.identifier8, 7, 11225-11229
dc.identifier19405901
dc.identifierhttps://hdl.handle.net/20.500.12728/5481
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5142730
dc.languageen
dc.publisherE-Century Publishing Corporation
dc.subject3'Untranslated region
dc.subjectC20209T
dc.subjectMutation
dc.subjectProthrombin
dc.subjectThrombophilia
dc.subjectacenocoumarol
dc.subjectlow molecular weight heparin
dc.subjectprothrombin
dc.subject3' untranslated region
dc.subjectadult
dc.subjectamplicon
dc.subjectArticle
dc.subjectcase report
dc.subjectdeep vein thrombosis
dc.subjectgene frequency
dc.subjectgene mutation
dc.subjectgenetic screening
dc.subjecthuman
dc.subjectmale
dc.subjectmiddle aged
dc.subjectmyalgia
dc.subjectreal time polymerase chain reaction
dc.titleProthrombin C20209T mutation in deep vein thrombosis: A case report
dc.typeArticle


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