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

Basit Öğe Kaydı
dc.authoridAYKUT, Ayça/0000-0002-1460-0053
dc.authoridIşık, Esra/0000-0003-0657-2408
dc.authoridEren, Erdal/0000-0002-1684-1053
dc.authoridGul Siraz, Ulku/0000-0001-7708-3498
dc.authoridPAPATYA ÇAKIR, ESRA DENİZ/0000-0003-4664-7435
dc.authoridAykut, Ayca/0000-0002-1460-0053
dc.authorwosidAYKUT, Ayça/ABH-6257-2020
dc.authorwosidIşık, Esra/AAE-3148-2021
dc.authorwosidEren, Erdal/JPK-3909-2023
dc.authorwosidyildirim, ruken/G-8137-2018
dc.authorwosidGul Siraz, Ulku/AAL-1515-2021
dc.authorwosidPAPATYA ÇAKIR, ESRA DENİZ/GQO-9634-2022
dc.authorwosidAykut, Ayca/B-1698-2018
dc.contributor.authorOzkinay, F.
dc.contributor.authorIsik, E.
dc.contributor.authorSimsek, D. G.
dc.contributor.authorAykut, A.
dc.contributor.authorKaraca, E.
dc.contributor.authorOzen, S.
dc.contributor.authorBolat, H.
dc.date.accessioned2024-06-12T11:24:06Z
dc.date.available2024-06-12T11:24:06Z
dc.date.issued2018
dc.departmentTrakya Üniversitesien_US
dc.description50th European-Society-of-Human-Genetics (ESHG) Conference -- MAY 27-30, 2017 -- Copenhagen, DENMARKen_US
dc.description.abstract[Abstract Not Available]en_US
dc.description.sponsorshipEuropean Soc Human Geneten_US
dc.identifier.endpage209en_US
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.startpage208en_US
dc.identifier.urihttps://hdl.handle.net/20.500.14551/26800
dc.identifier.volume26en_US
dc.identifier.wosWOS:000489312601184en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.relation.ispartofEuropean Journal Of Human Geneticsen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject[No Keywords]en_US
dc.titleMutation spectrum of GCK, HNF1A and HNF1B in MODY patients and 40 novel mutationsen_US
dc.typeConference Objecten_US

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