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  • The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome

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Original article
The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome

Authors

  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
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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
Journal of Medical Genetics 2009;46:447-450.

Publication history

  • Received November 13, 2008
  • Accepted February 21, 2009
  • First published May 11, 2009.
Online issue publication 
April 27, 2016

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2009 BMJ Publishing Group Ltd