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The association of single nucleotide polymorphism in human ABCA2 gene with gallstone disease / 中华肝胆外科杂志
Chinese Journal of Hepatobiliary Surgery ; (12): 718-721, 2011.
Article Dans Chinois | WPRIM | ID: wpr-421670
ABSTRACT
ObjectiveTo investigate the single nucleotide polymorphisms (SNPS) in the coding regions of the human ABCA2 gene and to determine the association of some of these SNPs with gallstone disease in a Chinese population. MethodsThe exons and part of the introns of the ABCA2 gene were sequenced using a fluorescent labeling automatic method in 24 patients with gallstone disease to identify and characterize the SNPs in a Chinese population. For SNPs in the exons, case-control studies were performed on patients and controls. ResultsTwelve SNPs were found within a 16911 bp region of the ABCA2 gene. Among them, two were in the exons, ten in the introns and five were novel SNPs. There was no significant difference in the SNPs genotype between the patients and the controis. ConclusionsThere is an important ethnic difference in the SNPs distribution of the human ABCA2 gene. The distribution of SNPs in the coding regions of the human ABCA2 gene is not significantly different between the patients and the controls.

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Type d'étude: Étude observationnelle / Facteurs de risque langue: Chinois Texte intégral: Chinese Journal of Hepatobiliary Surgery Année: 2011 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Type d'étude: Étude observationnelle / Facteurs de risque langue: Chinois Texte intégral: Chinese Journal of Hepatobiliary Surgery Année: 2011 Type: Article