Heterozygous large deletion mimicking homozygous substitution in MCFD2 in a patient with combined Factor V and Factor VIII deficiency

Haemophilia. 2024 Jul;30(4):1089-1091. doi: 10.1111/hae.15038. Epub 2024 May 19.
No abstract available

Publication types

  • Letter
  • Case Reports

MeSH terms

  • Factor V Deficiency* / genetics
  • Female
  • Hemophilia A* / genetics
  • Heterozygote*
  • Homozygote*
  • Humans
  • Male
  • Sequence Deletion
  • Vesicular Transport Proteins

Substances

  • MCFD2 protein, human
  • Vesicular Transport Proteins