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An insertion-deletion polymorphism in the interferon regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases.

par Dideberg, Vinciane;Kristjansdottir, Gudlaug;Milani, Lili;Libioulle, C;Sigurdsson, Snaevar;Louis, Edouard;Wiman, Ann-Christin;Vermeire, Séverine;Rutgeerts, Paul;Belaiche, Jacques;Franchimont, Denis ;Van Gossum, André ;Bours, Vincent;Syvänen, Ann-Christine
Référence Human molecular genetics, 16, 24, page (3008-3016)
Publication Publié, 2007-12

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Titre:	An insertion-deletion polymorphism in the interferon regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases.
Auteur:	Dideberg, Vinciane; Kristjansdottir, Gudlaug; Milani, Lili; Libioulle, C; Sigurdsson, Snaevar; Louis, Edouard; Wiman, Ann-Christin; Vermeire, Séverine; Rutgeerts, Paul; Belaiche, Jacques; Franchimont, Denis; Van Gossum, André; Bours, Vincent; Syvänen, Ann-Christine
Informations sur la publication:	Human molecular genetics, 16, 24, page (3008-3016)
Statut de publication:	Publié, 2007-12
Sujet CREF:	Sciences bio-médicales et agricoles
MeSH keywords:	Base Sequence
	Case-Control Studies
	Cohort Studies
	Gene Frequency
	Genetic Predisposition to Disease
	Humans
	INDEL Mutation
	Inflammatory Bowel Diseases -- genetics
	Interferon Regulatory Factors -- genetics
	Linkage Disequilibrium
	Polymorphism, Genetic
	Risk
Note générale:	Comparative Study
	Journal Article
	Multicenter Study
	Research Support, Non-U.S. Gov't
Langue:	Anglais
Identificateurs:	urn:issn:0964-6906
	info:doi/10.1093/hmg/ddm259
	info:pii/ddm259
	info:scp/36249002287
	info:pmid/17881657