2 Molecular basis of von Willebrand disease
- 1 June 1996
- journal article
- review article
- Published by Elsevier in Bailliere's Clinical Haematology
- Vol. 9 (2) , 229-241
- https://doi.org/10.1016/s0950-3536(96)80060-6
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Effects of different amino-acid substitutions in the leucine 694-proline 708 segment of recombinant von Willebrand factorBritish Journal of Haematology, 1995
- Identification of two mutations (Arg611Cys and Arg611His) in the A1 loop of von Willebrand factor (vWF) responsible for type 2 von Willebrand disease with decreased platelet-dependent function of vWF [see comments]Blood, 1995
- Characterization of von Willebrand factor gene defects in two unrelated patients with type IIC von Willebrand diseaseBlood, 1994
- Leu 697-->Val mutation in mature von Willebrand factor is responsible for type IIB von Willebrand diseaseBlood, 1994
- In-frame deletion of von Willebrand factor A domains in a dominant type of von Willebrand diseaseHuman Molecular Genetics, 1993
- Recessive inheritance of von Willebrand's disease type IThe Lancet, 1993
- Von Willebrand Disease: A Database of Point Mutations, Insertions, and DeletionsThrombosis and Haemostasis, 1993
- A stop codon in a patient with severe type III von Willebrand disease [letter]Blood, 1991
- Epitope mapping of the von Willebrand factor subunit distinguishes fragments present in normal and type IIA von Willebrand disease from those generated by plasmin.Journal of Clinical Investigation, 1987
- Human von Willebrand Factor (vWF): Isolation of Complementary DNA (cDNA) Clones and Chromosomal LocalizationScience, 1985