Pooled Sequencing of 531 Genes in Inflammatory Bowel Disease Identifies an Associated Rare Variant in BTNL2 and Implicates Other Immune Related Genes

The contribution of rare coding sequence variants to genetic susceptibility in complex disorders is an important but unresolved question. Most studies thus far have investigated a limited number of genes from regions which contain common disease associated variants. Here we investigate this in infla...

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Detalles Bibliográficos
Autores principales: Prescott, Natalie J., Lehne, Benjamin, Stone, Kristina, Lee, James C., Taylor, Kirstin, Knight, Jo, Papouli, Efterpi, Mirza, Muddassar M., Simpson, Michael A., Spain, Sarah L., Lu, Grace, Fraternali, Franca, Bumpstead, Suzannah J., Gray, Emma, Amar, Ariella, Bye, Hannah, Green, Peter, Chung-Faye, Guy, Hayee, Bu’Hussain, Pollok, Richard, Satsangi, Jack, Parkes, Miles, Barrett, Jeffrey C., Mansfield, John C., Sanderson, Jeremy, Lewis, Cathryn M., Weale, Michael E., Schlitt, Thomas, Mathew, Christopher G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335459/
https://www.ncbi.nlm.nih.gov/pubmed/25671699
http://dx.doi.org/10.1371/journal.pgen.1004955

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335459/
https://www.ncbi.nlm.nih.gov/pubmed/25671699
http://dx.doi.org/10.1371/journal.pgen.1004955

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