Thromb Haemost 1999; 82(04): 1373-1375
DOI: 10.1055/s-0037-1614402
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