English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/33493
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:

Title

Differential association of two PTPN22 coding variants with Crohn’s disease and ulcerative colitis

AuthorsDíaz-Gallo, L. M.; Gómez-García, M.; Mendoza, Juan L.; Taxonera, Carlos; Nieto, M. Ángela ; López-Nevot, Miguel-Ángel; Alizadeh, B. Z.; Martín, J.
Issue Date25-Nov-2010
PublisherBioMed Central
CitationJournal of Translational Medicine 8(S1): P2 (2010)
AbstractThe PTPN22 gene is an important risk factor for human autoimmunity. Two PTPN22 missense-SNPs, both with functional influence, the R620W (1858C>T, rs2476601) in exon 14 and the R263Q (788G>A, rs33996649) in exon 10 have been associated with autoimmune diseases [1-4].
Description2 páginas.-- Póster presentado al 5º European Workshop on Immune-Mediated Inflammatory Diseases celebrado en Sitges (Barcelona) dxel 1 al 3 de Diciembre de 2010.-- et al.
Publisher version (URL)http://dx.doi.org/10.1186/1479-5876-8-S1-P2
URIhttp://hdl.handle.net/10261/33493
DOI10.1186/1479-5876-8-S1-P2
ISSN1479-5876
Appears in Collections:(IPBLN) Artículos
Files in This Item:
File Description SizeFormat 
1479-5876-8-S1-P2.pdf171,89 kBAdobe PDFThumbnail
View/Open
Show full item record
Review this work
 


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.