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De novo and rare mutations in the HSPA1L heat shock gene associated with inflammatory bowel disease
BACKGROUND: Inflammatory bowel disease (IBD) is a chronic, relapsing inflammatory disease of the gastrointestinal tract which includes ulcerative colitis and Crohn's disease. Genetic risk factors for IBD are not well understood. METHODS: We performed a family-based whole exome sequencing (WES)...
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| 出版年: | Genome Med |
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| 主要な著者: | , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5270254/ https://ncbi.nlm.nih.gov/pubmed/28126021 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-016-0394-9 |
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