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Please use this identifier to cite or link to this item: http://hdl.handle.net/10400.18/1020

Título: CHIT1 genetic defects in the Portuguese population
Autor: Duarte, Ana
Ribeiro, Diogo
Amaral, Olga
Palavras-chave: Doenças Genéticas
Doenças Metabólicas
CHIT1
SNP
Frequency
Issue Date: 5-Sep-2012
Editora: Elsevier
Citação: Blood Cells Mol Dis. 2012 Sep 5. [Epub ahead of print]
Resumo: Chitotriosidase 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.
Descrição: AD e DR: bolseiros FCT.
Arbitragem científica: yes
URI: http://hdl.handle.net/10400.18/1020
ISSN: 1079-9796
Versão do Editor: http://www.sciencedirect.com/science/article/pii/S1079979612001593
Appears in Collections:DGH - Artigos em revistas internacionais

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