Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/7053
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dc.contributor.authorKecmanović, Miljanaen_US
dc.contributor.authorJović, N.en_US
dc.contributor.authorKeckarević-Marković, Milicaen_US
dc.contributor.authorDobričić, V.en_US
dc.contributor.authorKeckarević, Dušanen_US
dc.contributor.authorIgnjatović, P.en_US
dc.contributor.authorRomac, S.en_US
dc.date.accessioned2024-01-17T08:49:50Z-
dc.date.available2024-01-17T08:49:50Z-
dc.date.issued2008-06-07-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/7053-
dc.descriptionvol.255 pp.102-103en_US
dc.titleMutations in NHLRC1 gene are predominant cause of Lafora disease in Serbian populationen_US
dc.typeConference Paperen_US
dc.relation.conferenceEighteenth Meeting of the European Neurological Society, Nice, Franceen_US
dc.description.rankM34en_US
item.openairetypeConference Paper-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.orcid0000-0002-0182-8817-
crisitem.author.orcid0000-0001-9866-9439-
crisitem.author.orcid0000-0003-2446-7177-
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