The homozygous variant p.Gln1311* in exon 28 of VWF is associated with the development of alloantibodies in 3 unrelated patients with type 3 VWD

Haemophilia. 2021 Jul;27(4):e491-e494. doi: 10.1111/hae.14207. Epub 2021 Jan 6.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adolescent
  • Child
  • Exons / genetics
  • Female
  • Humans
  • Isoantibodies
  • Male
  • von Willebrand Disease, Type 3*
  • von Willebrand Diseases* / genetics
  • von Willebrand Factor / genetics

Substances

  • Isoantibodies
  • von Willebrand Factor