Publication:
Mutation spectrum of GCK, HNF1A and HNF1B in MODY patients and 40 novel mutations

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dc.contributor.authorÖzkınay, F.
dc.contributor.authorIşık, E.
dc.contributor.authorŞimşek, D. G.
dc.contributor.authorAykut, A.
dc.contributor.authorKaraca, E.
dc.contributor.authorÖzen, S.
dc.contributor.authorBolat, H.
dc.contributor.authorAtik, T.
dc.contributor.authorSaygılı, F.
dc.contributor.authorKartal, E.
dc.contributor.authorGül, U.
dc.contributor.authorAnik, A.
dc.contributor.authorTütüncüler, F.
dc.contributor.authorEren, Erdal
dc.contributor.authorÖzbek, M. N.
dc.contributor.authorBober, E.
dc.contributor.authorAbacı, A.
dc.contributor.authorKirel, B.
dc.contributor.authorErsoy, B.
dc.contributor.authorBüyükınan, M.
dc.contributor.authorKara, C.
dc.contributor.authorÇakır, E. P.
dc.contributor.authorYıldırım, R.
dc.contributor.authorİşgüven, P.
dc.contributor.authorDağdeviren, A.
dc.contributor.authorAğladıoğlu, S. Y.
dc.contributor.authorDoğan, M.
dc.contributor.authorSangun, O.
dc.contributor.authorArslanoğlu, I.
dc.contributor.authorKorkmaz, H. A.
dc.contributor.authorTemiz, F.
dc.contributor.authorOnay, H.
dc.contributor.buuauthorÖZÇELİK, ENDER EREN
dc.contributor.buuauthorEREN, ERDAL
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Pediatri ve Endokrinoloji Bölümü
dc.contributor.orcid0000-0002-1684-1053
dc.contributor.researcheridJPK-3909-2023
dc.date.accessioned2024-07-25T13:00:12Z
dc.date.available2024-07-25T13:00:12Z
dc.date.issued2018-10-01
dc.descriptionBu 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.sponsorshipEuropean Soc Human Genet
dc.identifier.eissn1476-5438
dc.identifier.endpage209
dc.identifier.issn1018-4813
dc.identifier.startpage208
dc.identifier.urihttps://hdl.handle.net/11452/43449
dc.identifier.volume26
dc.identifier.wos000489312601184
dc.indexed.wosWOS.SCI
dc.indexed.wosWOS.ISTP
dc.language.isoen
dc.publisherNature Publishing Group
dc.relation.journalEuropean Journal of Human Genetics
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectBiochemistry & molecular biology
dc.subjectGenetics & heredity
dc.titleMutation spectrum of GCK, HNF1A and HNF1B in MODY patients and 40 novel mutations
dc.typeMeeting Abstract
dspace.entity.typePublication
relation.isAuthorOfPublication76f45de0-4d66-4a33-8520-4f292004b0c7
relation.isAuthorOfPublication2d1c6521-88a9-4270-9918-92f16f98006c
relation.isAuthorOfPublication.latestForDiscovery76f45de0-4d66-4a33-8520-4f292004b0c7

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