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

Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.

Thromb Haemost 1998; 79(01): 240
DOI: 10.1055/s-0037-1614208

Letters to the Editor

Schattauer GmbH

Authors

Mohammad S. Enayat

¹From the Department of Haematology, Birmingham Children’s Hospital NHS Trust, Birmingham
Bimal D. M. Theophilus

¹From the Department of Haematology, Birmingham Children’s Hospital NHS Trust, Birmingham
Frank G. H. Hill

¹From the Department of Haematology, Birmingham Children’s Hospital NHS Trust, Birmingham
Peter E. Rose

²From the Pathology Department, South Warwickshire General Hospitals NHS Trust Warwick
Doris Culpan

³From the University of Bristol, Department of Pathology and Microbiology, Homeopathic Hospital Site
Jeffery Bidwell

³From the University of Bristol, Department of Pathology and Microbiology, Homeopathic Hospital Site
Graham R. Standen

⁴Department of Haematology, Bristol Royal Infirmary, Bristol, UK

Received 20. Juni 1997

Accepted after revision 09. September 1997

Publikationsdatum:
08. Dezember 2017 (online)

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.

Reference Link Ris
Crossref PubMed Suche in Google Scholar
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.

Reference Link Ris
Thieme Connect PubMed Suche in Google Scholar