Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/7040
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dc.contributor.authorKeckarević-Marković, Milicaen_US
dc.contributor.authorKecmanović, Miljanaen_US
dc.contributor.authorKeckarević, Dušanen_US
dc.contributor.authorMladenović, J.en_US
dc.contributor.authorMilić-Rasić, V.en_US
dc.contributor.authorRomac, S.en_US
dc.date.accessioned2024-01-16T11:40:57Z-
dc.date.available2024-01-16T11:40:57Z-
dc.date.issued2012-09-08-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/7040-
dc.descriptionEur J Neurol 19 (Suppl. 1), p. 786en_US
dc.titleFounder R32G mutation in GJB1 gene of Serbian CMT patientsen_US
dc.typeConference Paperen_US
dc.relation.conferenceThe 16th Congress of the European Federation of Neurological Societies, Stockholm, Swedenen_US
dc.description.rankM34en_US
item.cerifentitytypePublications-
item.openairetypeConference Paper-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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.orcid0000-0001-9866-9439-
crisitem.author.orcid0000-0002-0182-8817-
crisitem.author.orcid0000-0003-2446-7177-
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