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CHIT1 genetic defects in the Portuguese population

dc.contributor.authorDuarte, Ana
dc.contributor.authorRibeiro, Diogo
dc.contributor.authorAmaral, Olga
dc.date.accessioned2012-10-24T13:59:11Z
dc.date.available2012-10-24T13:59:11Z
dc.date.issued2012-09-05
dc.descriptionAD e DR: bolseiros FCT.por
dc.description.abstractChitotriosidase is an enzyme secreted by activated macrophages and a useful biomarker in several lysosomal and nonlysosomal diseases. However, chitotriosidase gene (CHIT1) mutations may lead to inaccuracy in the significance of this biomarker. Reports on the molecular spectrum of genetic variation in chitotriosidase are rare, and this is one of the few that focus on a specific population group. In this work we assessed the variation of CHIT1 mutations in ten normal controls and detected six missense alterations. G102S, a polymorphism with known altered catalytic properties, was the most frequent being detected in 4/10 individuals. Using allelic discrimination we tested 503 individuals, randomly sampled from the Portuguese population. Variant G102S was detected in 49.5% of the individuals and presented an allele frequency of 0.29. The results of this study showed that variability in CHIT1 gene is considerable and that G102S polymorphism presents a high frequency in the Portuguese.por
dc.description.sponsorshipFinanced by national funds through the FCT/MCTES. Project PIC/IC/82822/2007 (2009).por
dc.identifier.citationBlood Cells Mol Dis. 2012 Sep 5. [Epub ahead of print]por
dc.identifier.issn1079-9796
dc.identifier.otherdoi:10.1016/j.bcmd.2012.08.008
dc.identifier.urihttp://hdl.handle.net/10400.18/1020
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherElsevierpor
dc.relationFCT: PIC/IC/82822/2007por
dc.relation.publisherversionhttp://www.sciencedirect.com/science/article/pii/S1079979612001593por
dc.subjectDoenças Genéticaspor
dc.subjectDoenças Metabólicaspor
dc.subjectCHIT1por
dc.subjectSNPpor
dc.subjectFrequencypor
dc.titleCHIT1 genetic defects in the Portuguese populationpor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.titleBlood Cells, Molecules and Diseasespor
rcaap.rightsrestrictedAccesspor
rcaap.typearticlepor

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