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Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome

Celia J. Fang, Veronique Fremeaux-Bacchi, M. Kathryn Liszewski, Gaia Pianetti, Marina Noris, Timothy H. J. Goodship and John P. Atkinson

Article Information

Citation 
vol. 111 no. 2 624-632
PubMed 

Print ISSN 
Online ISSN 
History 
  • Submitted April 10, 2007
  • Accepted September 19, 2007
  • Published online January 8, 2008.

Article Versions


Contributors 
  • Celia J. Fang, 1Department of Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, MO;
  • Veronique Fremeaux-Bacchi, 2Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Service d'Immunologie Biologique, Paris, France;
  • M. Kathryn Liszewski, 1Department of Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, MO;
  • Gaia Pianetti, 3Mario Negri Institute for Pharmacological Research, Clinical Research Center for Rare Diseases, Aldo e Cele Daccò, Bergamo, Italy; and
  • Marina Noris, 3Mario Negri Institute for Pharmacological Research, Clinical Research Center for Rare Diseases, Aldo e Cele Daccò, Bergamo, Italy; and
  • Timothy H. J. Goodship, 4Institute of Human Genetics, University of Newcastle upon Tyne, Newcastle upon Tyne, United Kingdom
  • John P. Atkinson, 1Department of Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, MO;

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