Browsing by Author "Epcacan, S."
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Conference Object Recurrence of the P.gly262asp Mutation and a Novel P.thr176_gln186 Deletion in Twelve Patients With Congenital Factor X Deficiency(Wiley-blackwell, 2011) Oner, A. F.; Epcacan, S.; Cairo, A.; Menegatti, M.; Akbayram, S.; Peyvandi, F.; Oner, A. F.
