Publication:
Mutation Spectrum of GCK, HNF1A, and HNF1B in MODY Patients and 40 Novel Mutations

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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.contributor.authorIDEren, Erdal/0000-0002-1684-1053
dc.date.accessioned2020-06-21T13:06:57Z
dc.date.available2020-06-21T13:06:57Z
dc.date.issued2018
dc.departmentOMÜen_US
dc.department-temp[Ozkinay, F. -- Isik, E. -- Atik, T.] Ege Univ, Fac Med, Dept Pediat, Subdiv Pediat Genet, Izmir, Turkey -- [Simsek, D. G. -- Ozen, S.] Ege Univ, Fac Med, Dept Pediat, Subdiv Pediat Endocrinol, Izmir, Turkey -- [Aykut, A. -- Karaca, E.en_US
dc.description50th European-Society-of-Human-Genetics (ESHG) Conference -- MAY 27-30, 2017 -- Copenhagen, DENMARKen_US
dc.description.abstract…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/20.500.12712/11433
dc.identifier.volume26en_US
dc.identifier.wosWOS:000489312601184
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.relation.journalEuropean Journal of Human Geneticsen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_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.typeConference Objecten_US
dspace.entity.typePublication

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