Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/53718
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dc.contributor.authorSahin, Yavuzen_US
dc.contributor.authorGüngör, Olcayen_US
dc.contributor.authorGormez, Zelihaen_US
dc.contributor.authorDemirci, Hüseyin Aliyaren_US
dc.contributor.authorErgüner, Bekiren_US
dc.contributor.authorGüngör, Gülayen_US
dc.contributor.authorDilber, Cengizen_US
dc.date.accessioned2023-11-07T10:46:48Z-
dc.date.available2023-11-07T10:46:48Z-
dc.date.issued2017en_US
dc.identifier.urihttps://hdl.handle.net/11499/53718-
dc.language.isoenen_US
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_US
dc.titleExome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsyen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s13760-016-0721-3-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Başka Kurum Yazarıen_US
dc.identifier.pmid27844444-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept08.02. Political Science and Public Administration-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:İktisadi ve İdari Bilimler Fakültesi Koleksiyonu
Tıp Fakültesi Koleksiyonu
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