You are here

  • Home
  • Archive
  • Volume 48, Issue 4
  • Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype

Article info

Article menu
Download PDFPDF
Original article
Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype

Authors

  1. Correspondence to Professor Steve Jeffery, Medical Genetics, St George's, University of London, St George's Hospital Medical School, Cranmer Terrace, London SW17 ORE, UK; sggt100{at}sgul.ac.uk
View Full Text

Citation

Ostergaard P, Simpson MA, Brice G, et al
Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype
Journal of Medical Genetics 2011;48:251-255.

Publication history

  • Received September 27, 2010
  • Revised November 2, 2010
  • Accepted November 7, 2010
  • First published January 25, 2011.
Online issue publication 
September 21, 2016

Article Versions

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

© 2011, 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.