Article info
Clinical and epidemiological research
Concise report
Genetic variation in VTCN1 (B7-H4) is associated with course of disease in juvenile idiopathic arthritis
- Correspondence to Dr Marco W Schilham, Department of Pediatrics, P3-P, Leiden University Medical Center, PO Box 9600, 2300RC, Leiden, The Netherlands; M.W.Schilham{at}lumc.nl
Citation
Genetic variation in VTCN1 (B7-H4) is associated with course of disease in juvenile idiopathic arthritis
Publication history
- Received August 16, 2013
- Revised October 29, 2013
- Accepted December 3, 2013
- First published December 17, 2013.
Online issue publication
April 30, 2014
Article Versions
- Previous version (17 December 2013).
- You are viewing the most recent version of this article.
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions