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

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.authorDagdeviren, A.
dc.date.accessioned2020-06-21T13:06:57Z
dc.date.available2020-06-21T13:06:57Z
dc.date.issued2018
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.urihttps://hdl.handle.net/20.500.12712/11433
dc.description50th European-Society-of-Human-Genetics (ESHG) Conference -- MAY 27-30, 2017 -- Copenhagen, DENMARKen_US
dc.descriptionEren, Erdal/0000-0002-1684-1053en_US
dc.descriptionWOS: 000489312601184en_US
dc.description.abstract…en_US
dc.description.sponsorshipEuropean Soc Human Geneten_US
dc.language.isoengen_US
dc.publisherNature Publishing Groupen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleMutation spectrum of GCK, HNF1A and HNF1B in MODY patients and 40 novel mutationsen_US
dc.typeconferenceObjecten_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume26en_US
dc.identifier.startpage208en_US
dc.identifier.endpage209en_US
dc.relation.journalEuropean Journal of Human Geneticsen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US


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