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How do we encounter rare factor deficiencies in children? Single-centre results from Turkey

dc.contributor.authorTugcu, Deniz
dc.contributor.authorAyaz, Nuray
dc.contributor.authorBaslar, Zafer
dc.contributor.authorAkıcı, Ferhan
dc.contributor.authorAydoğan, Gonul
dc.contributor.authorSen, Hulya S.
dc.contributor.authorAkçay, Arzu
dc.contributor.authorSalcıoglu, Zafer
dc.contributor.authorKeskindemirci, Gonca
dc.date.accessioned2021-03-04T08:14:49Z
dc.date.available2021-03-04T08:14:49Z
dc.identifier.citationTugcu D., Salcıoglu Z., Akçay A., Sen H. S. , Aydoğan G., Akıcı F., Keskindemirci G., Ayaz N., Baslar Z., "How do we encounter rare factor deficiencies in children? Single-centre results from Turkey", BLOOD COAGULATION & FIBRINOLYSIS, cilt.26, ss.145-151, 2015
dc.identifier.issn0957-5235
dc.identifier.otherav_624fc85a-fa68-4b93-863e-24e330478107
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/68482
dc.identifier.urihttps://doi.org/10.1097/mbc.0000000000000204
dc.description.abstractBackground Rare factor deficiencies (RFDs) are autosomal recessively inherited coagulation factor deficiencies encountered at a frequency of between one in 500 000 and one in two million.
dc.language.isoeng
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectHematoloji
dc.subjectHEMATOLOJİ
dc.subjectİç Hastalıkları
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.titleHow do we encounter rare factor deficiencies in children? Single-centre results from Turkey
dc.typeMakale
dc.relation.journalBLOOD COAGULATION & FIBRINOLYSIS
dc.contributor.department, ,
dc.identifier.volume26
dc.identifier.startpage145
dc.identifier.endpage151
dc.contributor.firstauthorID2255428


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