Variants in TRIM22 that Affect NOD2 Signaling Are Associated With Very Early Onset Inflammatory Bowel Disease

BACKGROUND & AIMS: Severe forms of inflammatory bowel disease (IBD) that develop in very young children can be caused by variants in a single gene. We performed whole-exome sequence (WES) analysis to identify genetic factors that might cause granulomatous colitis and severe perianal disease, wit...

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Bibliografiset tiedot
Julkaisussa:Gastroenterology
Päätekijät: Li, Qi, Lee, Cheng Hiang, Peters, Lauren A, Mastropaolo, Lucas A, Thoeni, Cornelia, Elkadri, Abdul, Schwerd, Tobias, Zhu, Jun, Zhang, Bin, Zhao, Yongzhong, Hao, Ke, Dinarzo, Antonio, Hoffman, Gabriel, Kidd, Brian A, Murchie, Ryan, Adham, Ziad Al, Guo, Conghui, Kotlarz, Daniel, Cutz, Ernest, Walters, Thomas D, Shouval, Dror S, Curran, Mark, Dobrin, Radu, Brodmerkel, Carrie, Snapper, Scott B, Klein, Christoph, Brumell, John H, Hu, Mingjing, Nanan, Ralph, Snanter-Nanan, Brigitte, Wong, Melanie, Le Deist, Francoise, Haddad, Elie, Roifman, Chaim M, Deslandres, Colette, Griffiths, Anne M, Gaskin, Kevin J, Uhlig, Holm H, Schadt, Eric E, Muise, Aleixo M
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2016
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4842103/
https://ncbi.nlm.nih.gov/pubmed/26836588
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1053/j.gastro.2016.01.031
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