NOD2/CARD15 gene polymorphisms in Crohn's disease: a genotype–phenotype analysis

OBJECTIVESThree recently identified NOD2/CARD15 mutations have been described associated with an increased susceptibility Crohn's disease (CD). Our aim was to examine the potential association of these NOD2 mutations with CD and different subsets of CD phenotypes in our population. METHODSTwo h...

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Veröffentlicht in:	European journal of gastroenterology & hepatology 2004-01, Vol.16 (1), p.55-62
Hauptverfasser:	Heresbach, Denis, Gicquel-Douabin, Véronique, Birebent, Brigitte, D'halluin, Pierre-Nicolas, Heresbach-Le Berre, Nathalie, Dreano, Stéphane, Siproudhis, Laurent, Dabadie, Alain, Gosselin, Michel, Mosser, Jean, Semana, Gilbert, Bretagne, Jean-François, Yaouanq, Jacqueline
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Aged Analysis of Variance Biological and medical sciences Carrier Proteins - genetics Child Crohn Disease - genetics Female Gastroenterology. Liver. Pancreas. Abdomen Gene Frequency Genetic Predisposition to Disease - genetics Granuloma - genetics Heterozygote Homozygote Humans Intracellular Signaling Peptides and Proteins Male Medical sciences Middle Aged Mutation - genetics Nod2 Signaling Adaptor Protein Other diseases. Semiology Polymorphism, Genetic - genetics Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
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