ATXN3, ATXN7, CACNA1A, and RAI1 genes and mitochondrial polymorphism a10398g did not modify age at onset in spinocerebellar ataxia type 2 patients from South America

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dc.contributor.authorGodeiro Junior, Clécio de Oliveira
dc.contributor.authorPereira, Fernanda S.
dc.contributor.authorMonte, Thais L.
dc.contributor.authorLocks-Coelho, Lucas D.
dc.contributor.authorSilva, Amanda S. P.
dc.contributor.authorBarsottini, Orlando
dc.contributor.authorPedroso, José L.
dc.contributor.authorCornejo-Olivas, Mario
dc.contributor.authorMazzetti, Pilar
dc.contributor.authorVargas, Fernando R.
dc.contributor.authorLima, Maria Angélica F. D.
dc.contributor.authorLinden Junior, Hélio van der
dc.contributor.authorToralles, Maria Betânia Pereira
dc.contributor.authorMedeiros, Paula F. V.
dc.contributor.authorRibeiro, Erlane
dc.contributor.authorBraga-Neto, Pedro
dc.contributor.authorSalarini, Diego
dc.contributor.authorCastilhos, Raphael M.
dc.contributor.authorPereira, Maria Luiza Saraiva
dc.contributor.authorJardim, Laura Bannach
dc.contributor.authorID0000-0002-4312-1633pt_BR
dc.date.accessioned2023-07-05T19:44:04Z
dc.date.available2023-07-05T19:44:04Z
dc.date.issued2015-04-14
dc.description.resumoThe spinocerebellar ataxia type 2 (SCA2) is a rare autosomal dominant neurodegenerative disease caused by expansions of a CAG repeat tract at ATXN2 gene. These repeats range from 22 to 31 CAG in normal alleles and from 32–34 to 64 and more, in expanded alleles. ATXN2 expansion accounts for around 50 % of the variability in age at onset (AO) of symptoms . Former studies reported that other genes may be responsible for small effects in SCA2 AO. The CAG repeats’ length (CAGn) at RAI1 gene would explain 4 % of the remaining variance in AO in 46 SCA2 patients with no clear-cut geographical origin. Two publications studied candidate genes among patients with highly discordant AO, from an original sample of 394 patients from Holguin, Cuba Their data pointed to the CAGn at CACNA1A gene [3] and to a polymorphism of the mitochondrial complex I A10398G (rs2853826) as modifiers of SCA2 AO. We have previously found that longer CAGn at ATXN3 gene were associated with earlier ages at onset in a former sample of 49 SCA2 patients from Brazil. SCA2 AO was associated with the CAGn at ATXN7 gene in a European cohort of 289 SCA2 patients but this association was not confirmed in a second cohort [6]. Since replications in additional, independent samples of patients are required to validate a genetic association, we aimed to investigate these same loci in a South American cohort of SCA2 in order to add evidences on their role as modifiers of AO in this disease.pt_BR
dc.identifier.citationGODEIRO JUNIOR, Clecio de Oliveira et al. ATXN3, ATXN7, CACNA1A, and RAI1 Genes and Mitochondrial Polymorphism A10398G Did Not Modify Age at Onset in Spinocerebellar Ataxia Type 2 Patients from South America. The Cerebellum, [S.L.], v. 14, n. 6, p. 728-730, 14 abr. 2015. Springer Science and Business Media LLC. http://dx.doi.org/10.1007/s12311-015-0666-8. Disponível em: https://link.springer.com/article/10.1007/s12311-015-0666-8. Acesso em: 5 jul. 2023.pt_BR
dc.identifier.doihttps://doi.org/10.1007/s12311-015-0666-8
dc.identifier.urihttps://repositorio.ufrn.br/handle/123456789/53070
dc.languageenpt_BR
dc.publisherSpringerpt_BR
dc.subjectpolyglutaminept_BR
dc.subjectspinocerebellar ataxiapt_BR
dc.subjectA10398G polymorphismpt_BR
dc.subjectmaternal lineagept_BR
dc.subjectspinocerebellar ataxia typept_BR
dc.titleATXN3, ATXN7, CACNA1A, and RAI1 genes and mitochondrial polymorphism a10398g did not modify age at onset in spinocerebellar ataxia type 2 patients from South Americapt_BR
dc.typearticlept_BR

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