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Molecular genetic analysis of the F11 gene in 14 Turkish patients with factor XI deficiency: identification of novel and recurrent mutations and their inheritance within families
Çolakoğlu, Şeyma; Bayhan, Turan; Tavıl, Betül; Keskin Yılmaz, Ebru; Çakır, Volkan; Gümrük, Fatma; Çetin, Mualla; Aytaç, Selin; Berber, Ergül (Simti Servizi SRL, 2018)Background. Factor XI (FXI) deficiency is an autosomal bleeding disease associated with genetic defects in the F11 gene which cause decreased FXI levels or impaired FXI function. An increasing number of mutations has been ...
