Article info

Download PDFPDF
The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome
  1. Dr M-A Dragon-Durey, Service d’Immunologie Biologique, Hôpital Européen Georges Pompidou, 20 rue Leblanc, 75 015 Paris, France; marie-agnes.durey{at}egp.ap-hop-paris.fr
View Full Text

Citation

Dragon-Durey M, Blanc C, Marliot F, et al
The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome

Publication history

  • Received November 13, 2008
  • Accepted February 21, 2009
  • First published May 11, 2009.
Online issue publication 
July 01, 2009

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.