Publication: Mutation spectrum of GCK, HNF1A and HNF1B in MODY patients and 40 novel mutations
dc.contributor.author | Özkınay, F. | |
dc.contributor.author | Işık, E. | |
dc.contributor.author | Şimşek, D. G. | |
dc.contributor.author | Aykut, A. | |
dc.contributor.author | Karaca, E. | |
dc.contributor.author | Özen, S. | |
dc.contributor.author | Bolat, H. | |
dc.contributor.author | Atik, T. | |
dc.contributor.author | Saygılı, F. | |
dc.contributor.author | Kartal, E. | |
dc.contributor.author | Gül, U. | |
dc.contributor.author | Anik, A. | |
dc.contributor.author | Tütüncüler, F. | |
dc.contributor.author | Eren, Erdal | |
dc.contributor.author | Özbek, M. N. | |
dc.contributor.author | Bober, E. | |
dc.contributor.author | Abacı, A. | |
dc.contributor.author | Kirel, B. | |
dc.contributor.author | Ersoy, B. | |
dc.contributor.author | Büyükınan, M. | |
dc.contributor.author | Kara, C. | |
dc.contributor.author | Çakır, E. P. | |
dc.contributor.author | Yıldırım, R. | |
dc.contributor.author | İşgüven, P. | |
dc.contributor.author | Dağdeviren, A. | |
dc.contributor.author | Ağladıoğlu, S. Y. | |
dc.contributor.author | Doğan, M. | |
dc.contributor.author | Sangun, O. | |
dc.contributor.author | Arslanoğlu, I. | |
dc.contributor.author | Korkmaz, H. A. | |
dc.contributor.author | Temiz, F. | |
dc.contributor.author | Onay, H. | |
dc.contributor.buuauthor | ÖZÇELİK, ENDER EREN | |
dc.contributor.buuauthor | EREN, ERDAL | |
dc.contributor.department | Bursa Uludağ Üniversitesi/Tıp Fakültesi/Pediatri ve Endokrinoloji Bölümü | |
dc.contributor.orcid | 0000-0002-1684-1053 | |
dc.contributor.researcherid | JPK-3909-2023 | |
dc.date.accessioned | 2024-07-25T13:00:12Z | |
dc.date.available | 2024-07-25T13:00:12Z | |
dc.date.issued | 2018-10-01 | |
dc.description | Bu çalışma, 27-30, Mayıs 2017 tarihlerinde Copenhagen[Danimarka]’da düzenlenen 50. European-Society-of-Human-Genetics (ESHG) Conference Kongresi‘nde bildiri olarak sunulmuştur. | |
dc.description.sponsorship | European Soc Human Genet | |
dc.identifier.eissn | 1476-5438 | |
dc.identifier.endpage | 209 | |
dc.identifier.issn | 1018-4813 | |
dc.identifier.startpage | 208 | |
dc.identifier.uri | https://hdl.handle.net/11452/43449 | |
dc.identifier.volume | 26 | |
dc.identifier.wos | 000489312601184 | |
dc.indexed.wos | WOS.SCI | |
dc.indexed.wos | WOS.ISTP | |
dc.language.iso | en | |
dc.publisher | Nature Publishing Group | |
dc.relation.journal | European Journal of Human Genetics | |
dc.relation.publicationcategory | Konferans Öğesi - Uluslararası | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | Science & technology | |
dc.subject | Life sciences & biomedicine | |
dc.subject | Biochemistry & molecular biology | |
dc.subject | Genetics & heredity | |
dc.title | Mutation spectrum of GCK, HNF1A and HNF1B in MODY patients and 40 novel mutations | |
dc.type | Meeting Abstract | |
dspace.entity.type | Publication | |
relation.isAuthorOfPublication | 76f45de0-4d66-4a33-8520-4f292004b0c7 | |
relation.isAuthorOfPublication | 2d1c6521-88a9-4270-9918-92f16f98006c | |
relation.isAuthorOfPublication.latestForDiscovery | 76f45de0-4d66-4a33-8520-4f292004b0c7 |