Thromb Haemost 1999; 82(04): 1373-1375
DOI: 10.1055/s-0037-1614402
Letters to the Editor
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Null Alleles Are not a Common Cause of Type 1 von Willebrand Disease in the British Population

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
› Author Affiliations
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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