The Molecular Genetic Etiology by Whole Exome Sequence Analysis in Cases With Familial Type 1 Diabetes Mellitus without HLA Haplotype Predisposition or Incomplete Predisposition

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dc.contributor.authorYilmaz, Ugur Cem
dc.contributor.authorEvin, Ferda
dc.contributor.authorOnay, Huseyin
dc.contributor.authorOzen, Samim
dc.contributor.authorDarcan, Sukran
dc.contributor.authorGoksen, Damla
dc.date.accessioned2023-01-12T20:20:06Z
dc.date.available2023-01-12T20:20:06Z
dc.date.issued2021
dc.departmentN/A/Departmenten_US
dc.description.abstract[No Abstract Available]en_US
dc.identifier.endpage102en_US
dc.identifier.issn1663-2818
dc.identifier.issn1663-2826
dc.identifier.issn1663-2818en_US
dc.identifier.issn1663-2826en_US
dc.identifier.issueSUPPL 1en_US
dc.identifier.startpage101en_US
dc.identifier.urihttps://hdl.handle.net/11454/79295
dc.identifier.volume94en_US
dc.identifier.wosWOS:000696302600181en_US
dc.identifier.wosqualityQ1en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherKargeren_US
dc.relation.ispartofHormone Research In Paediatricsen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleThe Molecular Genetic Etiology by Whole Exome Sequence Analysis in Cases With Familial Type 1 Diabetes Mellitus without HLA Haplotype Predisposition or Incomplete Predispositionen_US
dc.typeConference Objecten_US

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