You are here

  • Home
  • Archive
  • Volume 71, Issue 6
  • Association between genetic variants in the tumour necrosis factor/lymphotoxin α/lymphotoxin β locus and primary Sjögren's syndrome in Scandinavian samples

Article info

Article menu
Download PDFPDF
Clinical and epidemiological research
Extended report
Association between genetic variants in the tumour necrosis factor/lymphotoxin α/lymphotoxin β locus and primary Sjögren's syndrome in Scandinavian samples

Authors

  1. Correspondence to Anne Isine Bolstad, Department of Clinical Dentistry – Periodontics, University of Bergen, Aarstadveien 17, N-5009 Bergen, Norway; anne.bolstad@iko.uib.no
View Full Text

Citation

Bolstad AI, Le Hellard S, Kristjansdottir G, et al
Association between genetic variants in the tumour necrosis factor/lymphotoxin α/lymphotoxin β locus and primary Sjögren's syndrome in Scandinavian samples
Annals of the Rheumatic Diseases 2012;71:981-988.

Publication history

  • Received July 12, 2011
  • Accepted December 11, 2011
  • First published January 30, 2012.
Online issue publication 
October 25, 2017

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