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 von 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.

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