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Rare coding variant analysis in a large cohort of Ashkenazi Jewish families with inflammatory bowel disease
Rare variants are thought to contribute to the genetics of inflammatory bowel disease (IBD), which is more common amongst the Ashkenazi Jewish (AJ) population. A family-based approach using exome sequencing of AJ individuals with IBD was employed with a view to identify novel rare genetic variants f...
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| Udgivet i: | Hum Genet |
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| Main Authors: | , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Springer Berlin Heidelberg
2018
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6153494/ https://ncbi.nlm.nih.gov/pubmed/30167848 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-018-1927-7 |
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