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.authorBolat, H.
dc.date.accessioned2024-04-24T17:50:00Z
dc.date.available2024-04-24T17:50:00Z
dc.date.issued2018
dc.departmentDicle 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/11468/23150
dc.identifier.volume26en_US
dc.identifier.wosWOS:000489312601184
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
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 Keyword]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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