Investigating the Genetic Basis of Type 3 of Von Willebrand Disease (VWD)
von Willebrand Disease (VWD) is the most common inherited bleeding disorder in humans, resulting from quantitative or qualitative deficiencies of von Willebrand factor (VWF). Type 3 VWD is the rarest and most severe form of the disease. This thesis characterizes the phenotype-genotype correlations o...
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| Language: | en en |
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2013
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| Online Access: | http://hdl.handle.net/1974/8426 |