Publication: A New Nationwide Initiative to Explore Genetic Variants in a Large Turkish Hereditary Neuropathy Cohort
| dc.authorwosid | Akinci, Gokhan/Hjp-0550-2023 | |
| dc.authorwosid | Ozyilmaz, Berk/U-5685-2019 | |
| dc.authorwosid | Ardicli, Didem/M-1586-2018 | |
| dc.authorwosid | Ünalp, Aycan/Ixd-3691-2023 | |
| dc.authorwosid | Polat, Ibrahim/A-7437-2018 | |
| dc.authorwosid | Dundar, Nihal/Aaf-9861-2021 | |
| dc.contributor.author | Akinci, G. | |
| dc.contributor.author | Ozyilmaz, B. | |
| dc.contributor.author | Parlar, O. | |
| dc.contributor.author | Unalp, A. | |
| dc.contributor.author | Polat, I. | |
| dc.contributor.author | Baydan, F. | |
| dc.contributor.author | Topaloglu, H. | |
| dc.contributor.authorID | Ünalp, Aycan/0000-0002-3611-5059 | |
| dc.contributor.authorID | Ozyilmaz, Berk/0000-0003-2654-3698 | |
| dc.date.accessioned | 2025-12-11T01:20:23Z | |
| dc.date.issued | 2023 | |
| dc.department | Ondokuz Mayıs Üniversitesi | en_US |
| dc.department-temp | [Akinci, G.; Parlar, O.; Unalp, A.; Polat, I.; Karaoglu, P.] Univ Hlth Sci, Izmir Fac Med, Behcet Uz Childrens Hosp, Dept Pediat Neurol, Izmir, Turkiye; [Ozyilmaz, B.] Univ Hlth Sci, Izmir Fac Med, Tepecik Training & Res Hosp, Genet Diag Ctr, Izmir, Turkiye; [Baydan, F.] Univ Hlth Sci, Tepecik Training Res Hosp, Dept Ped Neurol, Izmir, Turkiye; [Gazeteci, P.] Izmir Bakircay Univ, Cigli Training & Res Hosp, Dept Ped Neurol, Izmir, Turkiye; [Dundar, N. Olgac] Izmir Katip Celebi Univ, Dept Ped Neurol, Izmir, Turkiye; [Ardicli, D.] Ankara Bilkent City Hosp, Dept Pediat Neurol, Ankara, Turkiye; [Koken, O. Yayici] Akdeniz Univ, Dept Ped Neurol, Antalya, Turkiye; [Aksoy, A.] 19 Mayis Univ Hosp, Dept Ped Neurol, Samsun, Turkiye; [Komurcu, M.] Mersin Univ, Dept Ped Neurol, Mersin, Turkiye; [Cavusoglu, D.] Afyonkarahisar Hlth Sci Univ, Dept Ped Neurol Afyon, Afyonkarahisar, Turkiye; [Yis, U.] Dokuz Eylul Univ, Dept Pedeurol, Izmir, Turkiye; [Topaloglu, H.] Yeditepe Univ, Dept Ped Neurol, Istanbul, Turkiye | en_US |
| dc.description | Ünalp, Aycan/0000-0002-3611-5059; Ozyilmaz, Berk/0000-0003-2654-3698; | en_US |
| dc.description.woscitationindex | Science Citation Index Expanded - Conference Proceedings Citation Index - Science | |
| dc.identifier.doi | 10.1016/j.nmd.2023.07.478 | |
| dc.identifier.endpage | S188 | en_US |
| dc.identifier.issn | 0960-8966 | |
| dc.identifier.issn | 1873-2364 | |
| dc.identifier.scopusquality | Q3 | |
| dc.identifier.startpage | S188 | en_US |
| dc.identifier.uri | https://doi.org/10.1016/j.nmd.2023.07.478 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/43021 | |
| dc.identifier.volume | 33 | en_US |
| dc.identifier.wos | WOS:001087070800467 | |
| dc.identifier.wosquality | Q2 | |
| dc.language.iso | en | en_US |
| dc.publisher | Pergamon-Elsevier Science Ltd | en_US |
| dc.relation.ispartof | Neuromuscular Disorders | en_US |
| dc.relation.publicationcategory | Konferans Öğesi - Uluslararası - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.title | A New Nationwide Initiative to Explore Genetic Variants in a Large Turkish Hereditary Neuropathy Cohort | en_US |
| dc.type | Conference Object | en_US |
| dspace.entity.type | Publication |
