Systematic Association Mapping Identifies NELL1 as a Novel IBD Disease Gene

Crohn disease (CD), a sub-entity of inflammatory bowel disease (IBD), is a complex polygenic disorder. Although recent studies have successfully identified CD-associated genetic variants, these susceptibility loci explain only a fraction of the heritability of the disease. Here, we report on a multi...

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Detalles Bibliográficos
Autores principales: Franke, Andre, Hampe, Jochen, Rosenstiel, Philip, Becker, Christian, Wagner, Florian, Häsler, Robert, Little, Randall D., Huse, Klaus, Ruether, Andreas, Balschun, Tobias, Wittig, Michael, ElSharawy, Abdou, Mayr, Gabriele, Albrecht, Mario, Prescott, Natalie J., Onnie, Clive M., Fournier, Hélène, Keith, Tim, Radelof, Uwe, Platzer, Matthias, Mathew, Christopher G., Stoll, Monika, Krawczak, Michael, Nürnberg, Peter, Schreiber, Stefan
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1933598/
https://www.ncbi.nlm.nih.gov/pubmed/17684544
http://dx.doi.org/10.1371/journal.pone.0000691

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1933598/
https://www.ncbi.nlm.nih.gov/pubmed/17684544
http://dx.doi.org/10.1371/journal.pone.0000691

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