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Thromb Haemost 1998; 79(01): 240
DOI: 10.1055/s-0037-1614208
Letters to the Editor
Schattauer GmbH

A New (K1518E) Candidate Mutation Detected by Universal Heteroduplex Generator Analysis in a Patient with Type 2A (Phenotype IIA) von Willebrand Disease

Mohammad S. Enayat
1   From the Department of Haematology, Birmingham Children’s Hospital NHS Trust, Birmingham
,
Bimal D. M. Theophilus
1   From the Department of Haematology, Birmingham Children’s Hospital NHS Trust, Birmingham
,
Frank G. H. Hill
1   From the Department of Haematology, Birmingham Children’s Hospital NHS Trust, Birmingham
,
Peter E. Rose
2   From the Pathology Department, South Warwickshire General Hospitals NHS Trust Warwick
,
Doris Culpan
3   From the University of Bristol, Department of Pathology and Microbiology, Homeopathic Hospital Site
,
Jeffery Bidwell
3   From the University of Bristol, Department of Pathology and Microbiology, Homeopathic Hospital Site
,
Graham R. Standen
4   Department of Haematology, Bristol Royal Infirmary, Bristol, UK
› Author Affiliations
Further Information

Publication History

Received 20 June 1997

Accepted after revision 09 September 1997

Publication Date:
08 December 2017 (online)

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  • References

  • 1 Culpan D, Standen G, Wood N, Mazurier C, Gaucher C, Bidwell J. Rapid mutation screening in type 2A von Willebrand’s disease using universal heteroduplex generators.. Br J Haematol 1997; 96: 464-9.
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  • 2 Wood N, Standen G, Bowen D, Cumming A, Lush C, Lee R, Bidwell J. UHG-based mutation screening in type 2B von Willebrand’s disease: Detection of a candidate mutation Ser547Phe.. Thromb Haemost 1996; 75: 363-7.
    Article in Thieme ConnectPubMedGoogle Scholar