Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/2566
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dc.contributor.authorKeckarević, Dušanen_US
dc.contributor.authorStević, Zoricaen_US
dc.contributor.authorKeckarević Marković, Milicaen_US
dc.contributor.authorKecmanović, Miljanaen_US
dc.contributor.authorRomac, Stankaen_US
dc.date.accessioned2019-10-24T19:58:08Z-
dc.date.available2019-10-24T19:58:08Z-
dc.date.issued2012-02-
dc.identifier.issn1748-2968-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/2566-
dc.description.abstractAmyotrophic lateral sclerosis (ALS) is a fatal motor neuron disease in adults of unknown origin in most cases. Here we report a novel P66S mutation in exon 3 of the SOD1 gene in an apparently sporadic ALS patient with unusual early onset and rapid disease progression. Our data widen the spectrum of SOD1 mutations and clinical presentations of ALS. © 2012 Informa Healthcare.en_US
dc.language.isoenen_US
dc.relation.ispartofAmyotrophic Lateral Sclerosisen_US
dc.subjectAmyotrophic lateral sclerosisen_US
dc.subjectEarly onseten_US
dc.subjectExon 3 mutationen_US
dc.subjectRapid disease progressionen_US
dc.subjectSOD1en_US
dc.titleA novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progressionen_US
dc.typeArticleen_US
dc.identifier.doi10.3109/17482968.2011.627588-
dc.identifier.pmid22214314-
dc.identifier.scopus2-s2.0-84856612706-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84856612706-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.grantfulltextrestricted-
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.orcid0000-0003-2446-7177-
crisitem.author.orcid0000-0001-9866-9439-
crisitem.author.orcid0000-0002-0182-8817-
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