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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/130445
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dc.contributor.authorFranco, R. F.-
dc.contributor.authorMaffei, Francisco Humberto de Abreu-
dc.contributor.authorLourenco, D.-
dc.contributor.authorMorelli, V.-
dc.contributor.authorThomazini, I. A.-
dc.contributor.authorPiccinato, C. E.-
dc.contributor.authorTavella, M. H.-
dc.contributor.authorZago, M. A.-
dc.date.accessioned2014-05-27T11:19:31Z-
dc.date.accessioned2016-10-25T21:21:11Z-
dc.date.available2014-05-27T11:19:31Z-
dc.date.available2016-10-25T21:21:11Z-
dc.date.issued1998-01-01-
dc.identifierhttp://dx.doi.org/10.1046/j.1365-2141.1998.01051.x-
dc.identifier.citationBritish Journal of Haematology, v. 103, n. 3, p. 888-890, 1998.-
dc.identifier.issn0007-1048-
dc.identifier.urihttp://hdl.handle.net/11449/130445-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/130445-
dc.description.abstractWe investigated the prevalence of two reported mutations of the factor V gene (factor V Arg306 → Thr, or factor V Cambridge, and factor V Arg306 → Gly) in 104 relatively young patients with verified venous thrombosis and in 208 age-, sex- and race-matched controls, in order to establish whether the two mutations are associated with increased predisposition for venous thrombosis. PCR amplification followed by BstNI and MspI digestion was employed to determine the genotypes, and each mutation was confirmed by DNA sequencing. Among the controls, one individual was found to be heterozygous for the factor V Arg306 → Thr mutation and one heterozygous for the factor V Arg306 → Gly mutation; none of the patients carried either mutation. Our findings do not support factor V Cambridge and factor V Arg306 → Gly as risk factors for venous thrombosis.en
dc.format.extent888-890-
dc.publisherBlackwell Science-
dc.sourceScopus-
dc.subjectFactor V Arg306 → Gly-
dc.subjectFactor V Arg306 → Thr-
dc.subjectRisk factor-
dc.subjectThrombophilia-
dc.subjectVenous thrombosis-
dc.subjectBlood clotting factor 5-
dc.subjectAdolescent-
dc.subjectAdult-
dc.subjectAmino acid substitution-
dc.subjectChild-
dc.subjectDna sequence-
dc.subjectFemale-
dc.subjectGene mutation-
dc.subjectGenotype-
dc.subjectHeterozygosity-
dc.subjectHuman-
dc.subjectMajor clinical study-
dc.subjectMale-
dc.subjectPrevalence-
dc.subjectPriority journal-
dc.subjectVein thrombosis-
dc.subjectGenetic predisposition-
dc.subjectGenetics-
dc.subjectInfant-
dc.subjectMiddle aged-
dc.subjectMutation-
dc.subjectPreschool child-
dc.subjectRisk factor-
dc.subjectAdolescent-
dc.subjectAdult-
dc.subjectAmino Acid Substitution-
dc.subjectChild-
dc.subjectChild, Preschool-
dc.subjectFactor V-
dc.subjectFemale-
dc.subjectGenetic Predisposition to Disease-
dc.subjectHumans-
dc.subjectInfant-
dc.subjectMale-
dc.subjectMiddle Aged-
dc.subjectMutation-
dc.subjectRisk Factors-
dc.subjectVenous Thrombosis-
dc.titleFactor V Arg306 → Thr (factor V Cambridge) and factor V Arg306 → Gly mutations in venous thrombotic diseaseen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionFUNDHERP-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)-
dc.description.affiliationDepartment of Clinical Medicine Sch. of Med. of Ribeirão Preto USP, Ribeirão Preto-
dc.description.affiliationBlood Centre of Ribeirão Preto FUNDHERP, Ribeirão Preto-
dc.description.affiliationDepartment of Vascular Surgery School of Medicine of Botucatu UNESP-
dc.description.affiliationDepartment of Clinical Medicine UNIFESP-
dc.description.affiliationDepartment of Vascular Surgery Sch. of Med. of Ribeirão Preto USP, Ribeirão Preto-
dc.description.affiliationDepartment of Clinical Medicine Sch. of Med. of Ribeirão Preto University of São Paulo, 14048-900 Ribeirão Preto (SP)-
dc.description.affiliationUnespDepartment of Vascular Surgery School of Medicine of Botucatu UNESP-
dc.identifier.doi10.1046/j.1365-2141.1998.01051.x-
dc.identifier.wosWOS:000077457400047-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-0031593697.pdf-
dc.relation.ispartofBritish Journal of Haematology-
dc.identifier.scopus2-s2.0-0031593697-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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