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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Bibliografski detalji
Izdano u:Hum Genet
Glavni autori: 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
Jezik:Inglês
Izdano: Springer Berlin Heidelberg 2018
Teme:
Original Investigation
Online pristup: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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