Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci

BACKGROUND: Ulcerative colitis (UC), a complex polygenic disorder, is one of the main subphenotypes of inflammatory bowel disease. A comprehensive dissection of the genetic etiology of UC needs to assess the contribution of rare genetic variants including copy number variations (CNVs) to disease ris...

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Detalhes bibliográficos
Publicado no:BMC Med Genet
Main Authors: Saadati, Hamid Reza, Wittig, Michael, Helbig, Ingo, Häsler, Robert, Anderson, Carl A., Mathew, Christopher G., Kupcinskas, Limas, Parkes, Miles, Karlsen, Tom Hemming, Rosenstiel, Philip, Schreiber, Stefan, Franke, Andre
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2016
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4818401/
https://ncbi.nlm.nih.gov/pubmed/27037036
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-016-0289-z
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