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.

Authors :: ENAYAT, M. S.
GUILLIATT, A. M.
SHORT, P. E.
RASTEGAR-LARI, G.
JAZEBI, M.
RAVONBOD, S.
ALA, F.
CHAPMAN, O. G.
HILL, F. G. H.
Source :: Haemophilia; Nov2010, Vol. 16 Issue 6, p966-969, 4p, 1 Chart
Publication Year :: 2010
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.

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