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Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease
BACKGROUND: Inflammatory bowel disease (IBD) is an idiopathic, chronic disorder of unclear etiology with an underlying genetic predisposition. Recent genome-wide association studies have identified more than 200 IBD susceptibility loci, but the causes of IBD remain poorly defined. We hypothesized th...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | PLoS One |
|---|---|
| Prif Awduron: | , , , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Public Library of Science
2019
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6559655/ https://ncbi.nlm.nih.gov/pubmed/31185018 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0217846 |
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