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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
Author(s) -
ENAYAT M. S.,
GUILLIATT A. M.,
SHORT P. E.,
RASTEGARLARI G.,
JAZEBI M.,
RAVONBOD S.,
ALA F.,
CHAPMAN O. G.,
HILL F. G. H.
Publication year - 2010
Publication title -
haemophilia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.213
H-Index - 92
eISSN - 1365-2516
pISSN - 1351-8216
DOI - 10.1111/j.1365-2516.2010.02271.x
Subject(s) - haemophilia , medicine , hematology , haemophilia b , pediatrics , family medicine , haemophilia a