Characterization of the genetic basis of FXI deficiency in two Turkish patients

dc.contributor.author	Pekcelen, Y.
dc.contributor.author	Rimoldi, V.
dc.contributor.author	Berber, E.
dc.contributor.author	Usluer, S.
dc.contributor.author	Aksu, S.
dc.contributor.author	Caglayan, S. H.
dc.contributor.author	Duga, S.
dc.date.accessioned	2021-03-04T10:12:28Z
dc.date.available	2021-03-04T10:12:28Z
dc.date.issued	2010
dc.identifier.citation	Berber E., Rimoldi V., Usluer S., Aksu S., Pekcelen Y., Caglayan S. H. , Duga S., "Characterization of the genetic basis of FXI deficiency in two Turkish patients", HAEMOPHILIA, cilt.16, sa.3, ss.564-566, 2010
dc.identifier.issn	1351-8216
dc.identifier.other	av_6c0a4b07-f8e5-40cb-8d5d-d3b576d06804
dc.identifier.other	vv_1032021
dc.identifier.uri	http://hdl.handle.net/20.500.12627/74700
dc.identifier.uri	https://doi.org/10.1111/j.1365-2516.2009.02152.x
dc.language.iso	eng
dc.subject	HEMATOLOJİ
dc.subject	Hematoloji
dc.subject	İç Hastalıkları
dc.subject	Dahili Tıp Bilimleri
dc.subject	Sağlık Bilimleri
dc.subject	Tıp
dc.subject	Klinik Tıp (MED)
dc.subject	Klinik Tıp
dc.title	Characterization of the genetic basis of FXI deficiency in two Turkish patients
dc.type	Makale
dc.relation.journal	HAEMOPHILIA
dc.contributor.department	University of Milan , ,
dc.identifier.volume	16
dc.identifier.issue	3
dc.identifier.startpage	564
dc.identifier.endpage	566
dc.contributor.firstauthorID	196103

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