F8 intron 22 inversions and SNP rs73563631 in unrelated families with severe haemophilia A: clinical features and gene testing implications

Thromb Haemost. 2016 Mar;115(3):678-81. doi: 10.1160/TH15-08-0643. Epub 2015 Oct 22.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Chromosome Inversion
  • Factor VIII / chemistry*
  • Factor VIII / genetics*
  • Female
  • Gene Deletion
  • Genetic Linkage
  • Genetic Testing
  • Genotype
  • Hemophilia A / blood*
  • Hemophilia A / genetics*
  • Heterozygote
  • Humans
  • Introns
  • Male
  • Pedigree
  • Polymerase Chain Reaction
  • Polymorphism, Single Nucleotide*

Substances

  • Factor VIII