Recurrence of the P.gly262asp Mutation and a Novel P.thr176_gln186 Deletion in Twelve Patients With Congenital Factor X Deficiency

Oner, A. F.Epcacan, S.Cairo, A.Menegatti, M.Akbayram, S.Peyvandi, F.Oner, A. F.2025-05-102025-05-1020111538-79331538-7836https://hdl.handle.net/20.500.14720/17113eninfo:eu-repo/semantics/closedAccessRecurrence of the P.gly262asp Mutation and a Novel P.thr176_gln186 Deletion in Twelve Patients With Congenital Factor X DeficiencyConference Object9Q1Q1935936WOS:000208992804310