Thromb Haemost 1999; 82(04): 1373-1375
DOI: 10.1055/s-0037-1614402
Letters to the Editor
Schattauer GmbH

Null Alleles Are not a Common Cause of Type 1 von Willebrand Disease in the British Population

Authors

  • T. C. Coughlan

    1   From the Division of Molecular and Genetic Medicine, Royal Hallamshire Hospital, Sheffield, UK
  • J. L. Blagg

    1   From the Division of Molecular and Genetic Medicine, Royal Hallamshire Hospital, Sheffield, UK
  • M. Abulola

    1   From the Division of Molecular and Genetic Medicine, Royal Hallamshire Hospital, Sheffield, UK
  • M. E. Daly

    1   From the Division of Molecular and Genetic Medicine, Royal Hallamshire Hospital, Sheffield, UK
  • K. K. Hampton

    1   From the Division of Molecular and Genetic Medicine, Royal Hallamshire Hospital, Sheffield, UK
  • M. Makris

    1   From the Division of Molecular and Genetic Medicine, Royal Hallamshire Hospital, Sheffield, UK
  • I. R. Peake

    1   From the Division of Molecular and Genetic Medicine, Royal Hallamshire Hospital, Sheffield, UK
  • A. C. Goodeve

    1   From the Division of Molecular and Genetic Medicine, Royal Hallamshire Hospital, Sheffield, UK
Further Information

Publication History

Received 23 March 1999

Accepted after major revision 27 May 1999

Publication Date:
08 December 2017 (online)

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