Adam Dinan

Research Associate
University of Cambridge

Presentation(s):

• PB0823 - The rare VWF non-canonical splice-site variant, c.8155+6T>A, causes type 3 von Willebrand disease in homozygosity and results in perinuclear retention of VWF in endothelial cells

  Monday, July 11, 2022
  6:30 PM – 7:30 PM