Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/5750

Registo completo
Campo DCValorIdioma
dc.contributor.authorLima, M.-
dc.contributor.authorCosta, Maria do Carmo-
dc.contributor.authorMontiel, R.-
dc.contributor.authorFerro, Anabela-
dc.contributor.authorSantos, C.-
dc.contributor.authorSilva, C.-
dc.contributor.authorBettencourt, C.-
dc.contributor.authorSousa, Alda-
dc.contributor.authorSequeiros, Jorge-
dc.contributor.authorCoutinho, P.-
dc.contributor.authorMaciel, P.-
dc.date.accessioned2006-11-06T16:55:05Z-
dc.date.available2006-11-06T16:55:05Z-
dc.date.issued2005-
dc.identifier.citation"Human heredity". ISSN 0001-5652. 60:3 (2005) 156-163.eng
dc.identifier.issn0001-5652eng
dc.identifier.urihttps://hdl.handle.net/1822/5750-
dc.description.abstractTo gain insights on the molecular mechanisms of mutation that led to the emergence of expanded alleles in the MJD gene, by studying the behavior of wild-type alleles and testing the association of its distribution with the representation of the disease. Methods: The number of CAG motifs in the MJD gene was determined in a representative sample of 1000 unrelated individuals. Associations between the repeat size and the epidemiological representation of MJD were tested. Results: The allelic profi le of the total sample was in the normal range (13–41 repeats), with mode (CAG) 23 . No intermediate alleles were present. Allelic size distribution showed a negative skew. The correlation between the epidemiological representation of MJD in each district and the frequency of small, medium and large normal alleles was not signifi cant. Further correlations performed grouping the districts also failed to produce signifi cant results. Conclusions: The absence of association between the size of the repeats and the representation of MJD demonstrates that prevalence is not an indirect refl ection of the frequency of large normal alleles. Globally the results obtained are in accordance with a model that postulates the occurrence of a few mutations on the basis of most of the MJD cases worldwide.eng
dc.language.isoengeng
dc.publisherKarger AGpor
dc.rightsopenAccesseng
dc.subjectMachado-Joseph diseaseeng
dc.subjectExpansion disordereng
dc.subjectSCA3eng
dc.subjectMutational biaseng
dc.subjectTriplet repeatseng
dc.subjectPopulation studyeng
dc.subjectPortugaleng
dc.titlePopulation genetics of wild-type CAG repeats in the Machado-Joseph disease gene in Portugaleng
dc.typearticlepor
dc.peerreviewedyeseng
sdum.number3eng
sdum.pagination156–163eng
sdum.publicationstatuspublishedeng
sdum.volume60eng
oaire.citationStartPage156por
oaire.citationEndPage163por
oaire.citationIssue3por
oaire.citationVolume60por
dc.identifier.doi10.1159/000090035por
dc.identifier.pmid16340213por
dc.subject.wosScience & Technologypor
sdum.journalHuman Hereditypor
Aparece nas coleções:ICVS - Artigos em revistas internacionais / Papers in international journals

Ficheiros deste registo:
Ficheiro Descrição TamanhoFormato 
Maciel - Hum Her 2005.pdf237,58 kBAdobe PDFVer/Abrir

Partilhe no FacebookPartilhe no TwitterPartilhe no DeliciousPartilhe no LinkedInPartilhe no DiggAdicionar ao Google BookmarksPartilhe no MySpacePartilhe no Orkut
Exporte no formato BibTex mendeley Exporte no formato Endnote Adicione ao seu ORCID