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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Détails bibliographiques
Publié dans:Hum Genet
Auteurs principaux: Schiff, E. R., Frampton, M., Ben-Yosef, N., Avila, B. E., Semplici, F., Pontikos, N., Bloom, S. L., McCartney, S. A., Vega, R., Lovat, L. B., Wood, E., Hart, A., Israeli, E., Crespi, D., Furman, M. A., Mann, S., Murray, C. D., Segal, A. W., Levine, A. P.
Format: Artigo
Langue:Inglês
Publié: Springer Berlin Heidelberg 2018
Sujets:
Original Investigation
Accès en ligne: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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