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Thromb Haemost 1998; 80(01): 32-36
DOI: 10.1055/s-0037-1615134
Rapid Communication
Schattauer GmbH

Type 2N von Willebrand Disease: Rapid Genetic Diagnosis of G2811A (R854Q), C2696T (R816W), T2701A (H817Q) and G2823T (C858F) – Detection of a Novel Candidate Type 2N Mutation: C2810T (R854W)

Authors

  • D. J. Bowen

    1   Arthur Bloom Center, Dept of Haematology, University of Wales College of Medicine, Heath Park, Cardiff, S Wales, UK
  • G. R. Standen

    2   Molecular Haematology Unit, Dept of Haematology, Bristol Royal Infirmary, Bristol, UK
  • C. Mazurier

    3   Laboratoire de Recherche sur l’Hémostase, LFB, Lille, France
  • C. Gaucher

    3   Laboratoire de Recherche sur l’Hémostase, LFB, Lille, France
  • A. Cumming

    4   Dept of Clinical Haematology, The Royal Infirmary, Manchester, UK
  • S. Keeney

    4   Dept of Clinical Haematology, The Royal Infirmary, Manchester, UK
  • J. Bidwell

    5   Dept of Pathology and Microbiology, University of Bristol, Bristol, UK