Three factor 11 mutations associated with factor XI deficiency in a Turkish family

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dc.authoridVeysel Sabri Hançer / 0000-0003-2994-1077en_US
dc.authoridMurat Büyükdoğan / 0000-0001-7948-0235
dc.authorscopusidMurat Büyükdoğan / 35247676100
dc.authorscopusidVeysel Sabri Hançer / 6506533543
dc.authorwosidMurat Büyükdoğan / Y-2855-2018
dc.authorwosidVeysel Sabri Hançer / X-8971-2018
dc.contributor.authorHançer, Veysel Sabri
dc.contributor.authorGökgöz, Zafer
dc.contributor.authorBüyükdoğan, Murat
dc.date.accessioned2020-08-30T20:07:47Z
dc.date.available2020-08-30T20:07:47Z
dc.date.issued2018
dc.departmentİstinye Üniversitesien_US
dc.description.abstractFactor XI (FXI) is a homodimeric serine protease, which is produced in the liver and circulates in the plasma complexed with high-molecular-weight kininogen. FXI plays an important role in the amplification of the initial coagulation response via a positive feedback mechanism for the generation of additional thrombin [1,2,3,4]. Congenital FXI deficiency is characterized by decreased levels or activity of FXI in the plasma and may cause an inherited bleeding disorder. The FXI gene is located on 4q34- 35 and consists of 15 exons.en_US
dc.identifier.citationHancer, V. S., Gokgoz, Z., & Buyukdogan, M. (2018). Three Factor 11 Mutations Associated with Factor XI Deficiency in a Turkish Family. TURKISH JOURNAL OF HEMATOLOGY, 35(1), 79–80. https://doi.org/10.4274/tjh.2017.0140en_US
dc.identifier.doi10.4274/tjh.2017.0140en_US
dc.identifier.endpage80en_US
dc.identifier.issn1300-7777en_US
dc.identifier.issn1308-5263en_US
dc.identifier.issue1en_US
dc.identifier.pmid28947414en_US
dc.identifier.scopus2-s2.0-85042436343en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage79en_US
dc.identifier.trdizinid267216en_US
dc.identifier.urihttps://doi.org/10.4274/tjh.2017.0140
dc.identifier.urihttps://hdl.handle.net/20.500.12713/829
dc.identifier.volume35en_US
dc.identifier.wosWOS:000426572200016en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakTR-Dizinen_US
dc.indekslendigikaynakPubMeden_US
dc.institutionauthorHançer, Veysel Sabrien_US
dc.institutionauthorBüyükdoğan, Muraten_US
dc.language.isoenen_US
dc.publisherGalenos Yayinciliken_US
dc.relation.ispartofTurkish Journal of Hematologyen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectFactor Xien_US
dc.subjectMutationen_US
dc.subjectFamilyen_US
dc.titleThree factor 11 mutations associated with factor XI deficiency in a Turkish familyen_US
dc.typeLetteren_US

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