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Factor 8 Gene Mutation Spectrum of 270 Patients with Hemophilia A: Identification of 36 Novel Mutations

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dc.creator ATİK, TAHİR
dc.creator Ozkinay, Ferda
dc.creator Onay, Huseyin
dc.creator YILMAZ İNCE, Ebru
dc.creator Shamsali, Moharram
dc.creator BALKAN, CAN
dc.creator Oymak, Yesim
dc.creator Gunes, Adalet Meral
dc.creator Salcioglu, Zafer
dc.creator ALBAYRAK, CANAN
dc.creator ŞAHİN, FAHRİ
dc.creator Culha, Vildan
dc.creator IŞIK, ESRA
dc.creator Kupesiz, Alphan
dc.creator Belen, Fatma Burcu
dc.creator SEZGİN EVİM, MELİKE
dc.creator ÜNAL, EKREM
dc.creator Ozbek, Namik Yasar
dc.creator Baytan, Birol
dc.creator TÜYSÜZ KİNTRUP, GÜLEN
dc.creator Kavaklo, Kaan
dc.creator Gucer, Tuba Nur Tahtakesen
dc.creator Akgun, Bilcag
dc.date 2019-12-31T21:00:00Z
dc.date.accessioned 2021-01-21T09:10:51Z
dc.date.available 2021-01-21T09:10:51Z
dc.identifier f482710b-ddee-443b-b7d4-d8cd74b78aac
dc.identifier 10.4274/tjh.galenos.2020.2019.0262
dc.identifier https://avesis.sdu.edu.tr/publication/details/f482710b-ddee-443b-b7d4-d8cd74b78aac/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/89066
dc.description Objective: Hemophilia A (HA) is the most severe X-linked inherited bleeding disorder caused by hemizygous mutations in the factor 8 (F8) gene. The aim of this study is to determine the mutation spectrum of the F8 gene in a large HA cohort from Turkey, and then to establish a phenotype-genotype correlation.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Factor 8 Gene Mutation Spectrum of 270 Patients with Hemophilia A: Identification of 36 Novel Mutations
dc.type info:eu-repo/semantics/article


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