Identification of a novel mutation in the MCFD2 gene in a Tunisian family with combined factor V and VIII deficiency

Tunis Med. 2012 Apr;90(4):343-4.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Consanguinity
  • Factor V Deficiency / genetics*
  • Female
  • Hemophilia A / genetics*
  • Humans
  • Male
  • Mutation, Missense*
  • Sequence Analysis, DNA
  • Tunisia
  • Vesicular Transport Proteins / genetics*
  • Young Adult

Substances

  • MCFD2 protein, human
  • Vesicular Transport Proteins