Platelet morphological changes in 2 patients with von Willebrand disease type 3 caused by large homozygous deletions of the von Willebrand factor gene

Παρόμοια τεκμήρια

• Homozygous and heterozygous deletions of the von Willebrand factor gene in patients and carriers of severe von Willebrand disease.
  ανά: Ngo, K Y, κ.ά.
  Έκδοση: (1988)
• Premature termination codon mutations in the von Willebrand factor gene are associated with allele-specific and position-dependent mRNA decay
  ανά: Platè, Manuela, κ.ά.
  Έκδοση: (2010)
• Role of von Willebrand factor in the haemostasis
  ανά: Peyvandi, Flora, κ.ά.
  Έκδοση: (2011)
• Is the mysterious platelet receptor GPV an unsuspected major target for platelet autoantibodies?
  ανά: Nurden, Paquita, κ.ά.
  Έκδοση: (2019)
• An intracytoplasmic β3 Leu718 deletion in a patient with a novel platelet phenotype
  ανά: Nurden, Paquita, κ.ά.
  Έκδοση: (2017)