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Molecular investigation of pediatric portuguese patients with sensorineural hearing loss

dc.contributor.authorNogueira, C.
dc.contributor.authorCoutinho, M.
dc.contributor.authorPereira, C.
dc.contributor.authorTessa, A.
dc.contributor.authorSantorelli, F.M.
dc.contributor.authorVilarinho, L.
dc.date.accessioned2012-10-24T16:46:33Z
dc.date.available2012-10-24T16:46:33Z
dc.date.issued2011
dc.description.abstractThe understanding of the molecular genetics in sensorineural hearing loss (SNHL) has advanced rapidly during the last decade, but the molecular etiology of hearing impairment in the Portuguese population has not been investigated thoroughly. To provide appropriate genetic testing and counseling to families, we analyzed the whole mitochondrial genome in 95 unrelated children with SNHL (53 nonsyndromic and 42 syndromic) and searched for variations in two frequent genes, GJB2 and GJB6, in the non- syndromic patients. Mutations in mtDNA were detected in 4.2% of the cases, including a hitherto undescribed change in the mtDNA-tRNATrp gene (namely, m.5558A>G). We also identified mono- or biallelic GJB2 mutations in 20 of 53 non-syndromic cases and also detected two novel mutations (p.P70R and p.R127QfsX84). Our data further reinforce the notion that genetic heterogeneity is paramount in children with SNHL.por
dc.identifier.citationGenet Res Int. 2011;2011:587602. Epub 2011 Sep 25por
dc.identifier.issn2090-3154
dc.identifier.urihttp://hdl.handle.net/10400.18/1056
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherSAGE-Hindawi Access to Researchpor
dc.relation.publisherversionhttp://www.hindawi.com/journals/gri/2011/587602/por
dc.subjectSensorineural Hearing Losspor
dc.subjectDoenças Genéticaspor
dc.subjectmtDNApor
dc.titleMolecular investigation of pediatric portuguese patients with sensorineural hearing losspor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.startPage587602por
oaire.citation.titleGenetics Research Internationalpor
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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