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1. A novel alanine or threonine 789 to proline mutation causing type 2N von Willebrand's disease when inherited homozygously or heterozygously with arginine 854 to glutamine mutation LETTER TO THE EDITOR.

Author

ENAYAT, M. S., GUILLIATT, A. M., SHORT, P. E., RASTEGAR-LARI, G., JAZEBI, M., RAVONBOD, S., ALA, F., CHAPMAN, O. G., and HILL, F. G. H.

Subjects
LETTERS to the editor, VON Willebrand disease
Abstract

A letter to the editor is presented discussing the type 2N von Willebrand's disease (VWD) when inherited with arginine 854 to glutamine mutation.

Published
2010
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