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Expression of two type 2N von Willebrand disease mutations identified in exon 18 of von Willebrand factor gene

โœ Scribed by L. Hilbert; S. Jorieux; M. Fontenay-Roupie; M. Guicheteau; E. Fressinaud; D. Meyer; C. Mazurier; the INSERM Network on Molecular Abnormalities in von Willebrand Disease


Book ID
108672869
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
283 KB
Volume
127
Category
Article
ISSN
0007-1048

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Diagnosis of von Willebrand disease type
โœ Miller, Connie H.; Kelley, Leslie; Green, David ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 107 KB ๐Ÿ‘ 2 views

## Diagnosis of von Willebrand disease Type 2N (vWD 2N ), which mimics hemophilia A and its carrier state, is important for accurate genetic counseling and appropriate therapy. To make testing for the disorder more clinically applicable, we developed a simplified method for measurement of factor V