Omid Seidizadeh

Genetic determinants of low von Willebrand factor from whole exome sequencing

Low von Willebrand factor (VWF; 30–50 IU/dL) is a common clinical phenotype associated with bleeding, but its genetic basis remains poorly defined. We aimed to explore the contribution of rare and common variants to Low VWF and bleeding risk. Whole-exome sequencing was performed...

When genotype precedes phenotype: incidental findings in inherited disorders of hemostasis

Not available.