Author: "Ravonbod S" - Searchworks@Jio Institute Digital Library Search Results

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1. A novel alanine or threonine 789 to proline mutation causing type 2N von Willebrandʼs disease when inherited homozygously or heterozygously with arginine 854 to glutamine mutation

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.
Published: 2010
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