Thromb Haemost 2006; 95(01): 195-198
DOI: 10.1055/s-0037-1612584
Case Report
Schattauer GmbH

Prothrombin deficiency caused by compound heterozygosity for two novel mutations in the prothrombin gene associated with a bleeding tendency

Authors

  • Hristo Stanchev

    1   Departement of Pediatrics, Storstrømmens Sygehus, Næstved, Denmark
  • Malou Philips

    2   Department of Clinical Biochemistry, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
  • Bruno O. Villoutreix

    3   INSERM U648, University of Paris V, School of Pharmacy, Paris, France
  • Lise Aksglæde

    1   Departement of Pediatrics, Storstrømmens Sygehus, Næstved, Denmark
  • Stefan Lethagen

    4   Haemophilia Centre, Department of Pediatrics, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
    5   Department for Coagulation Disorders, Malmö University Hospital, Lund University, Malmö, Sweden
  • Sixtus Thorsen

    2   Department of Clinical Biochemistry, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
Further Information

Publication History

Received 12 May 2005

Accepted after resubmission 08 November 2005

Publication Date:
15 December 2017 (online)

Preview