Recurrence of the P.gly262asp Mutation and a Novel P.thr176_gln186 Deletion in Twelve Patients With Congenital Factor X Deficiency
| dc.authorwosid | Akbayram, Sinan/Aag-5737-2020 | |
| dc.authorwosid | Cairo, Andrea/Aac-7765-2022 | |
| dc.authorwosid | Peyvandi, Flora/Aak-7437-2020 | |
| dc.contributor.author | Oner, A. F. | |
| dc.contributor.author | Epcacan, S. | |
| dc.contributor.author | Cairo, A. | |
| dc.contributor.author | Menegatti, M. | |
| dc.contributor.author | Akbayram, S. | |
| dc.contributor.author | Peyvandi, F. | |
| dc.contributor.author | Oner, A. F. | |
| dc.date.accessioned | 2025-05-10T17:48:28Z | |
| dc.date.available | 2025-05-10T17:48:28Z | |
| dc.date.issued | 2011 | |
| dc.department | T.C. Van Yüzüncü Yıl Üniversitesi | en_US |
| dc.department-temp | [Oner, A. F.; Epcacan, S.; Akbayram, S.; Oner, A. F.] Yuzuncu Yil Univ, Dept Pediat Hematol, Sch Med, Van, Turkey; [Cairo, A.; Menegatti, M.; Peyvandi, F.] Univ Milan, A Bianchi Bonomi Hemophilia & Thrombosis Ctr, I-20122 Milan, Italy | en_US |
| dc.description.woscitationindex | Science Citation Index Expanded | |
| dc.identifier.endpage | 936 | en_US |
| dc.identifier.issn | 1538-7933 | |
| dc.identifier.issn | 1538-7836 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 935 | en_US |
| dc.identifier.uri | https://hdl.handle.net/20.500.14720/17113 | |
| dc.identifier.volume | 9 | en_US |
| dc.identifier.wos | WOS:000208992804310 | |
| dc.identifier.wosquality | Q1 | |
| dc.language.iso | en | en_US |
| dc.publisher | Wiley-blackwell | en_US |
| dc.relation.publicationcategory | Konferans Öğesi - Uluslararası - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.title | Recurrence of the P.gly262asp Mutation and a Novel P.thr176_gln186 Deletion in Twelve Patients With Congenital Factor X Deficiency | en_US |
| dc.type | Conference Object | en_US |