Please use this identifier to cite or link to this item:
https://hdl.handle.net/11499/53718
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Sahin, Yavuz | en_US |
dc.contributor.author | Güngör, Olcay | en_US |
dc.contributor.author | Gormez, Zeliha | en_US |
dc.contributor.author | Demirci, Hüseyin Aliyar | en_US |
dc.contributor.author | Ergüner, Bekir | en_US |
dc.contributor.author | Güngör, Gülay | en_US |
dc.contributor.author | Dilber, Cengiz | en_US |
dc.date.accessioned | 2023-11-07T10:46:48Z | - |
dc.date.available | 2023-11-07T10:46:48Z | - |
dc.date.issued | 2017 | en_US |
dc.identifier.uri | https://hdl.handle.net/11499/53718 | - |
dc.language.iso | en | en_US |
dc.rights | info:eu-repo/semantics/restrictedAccess | en_US |
dc.title | Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsy | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1007/s13760-016-0721-3 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Başka Kurum Yazarı | en_US |
dc.identifier.pmid | 27844444 | - |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
item.cerifentitytype | Publications | - |
item.openairetype | Article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.languageiso639-1 | en | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 08.02. Political Science and Public Administration | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
Appears in Collections: | İktisadi ve İdari Bilimler Fakültesi Koleksiyonu Tıp Fakültesi Koleksiyonu |
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