Genetic analysis in FXI deficient patients from northwestern Italy: three novel and one recurrent mutation

Eur J Haematol. 2013 Apr;90(4):351-3. doi: 10.1111/ejh.12072. Epub 2013 Feb 15.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Amino Acid Substitution
  • DNA Mutational Analysis
  • Factor XI Deficiency / blood
  • Factor XI Deficiency / genetics*
  • Female
  • Genetic Association Studies
  • Haplotypes
  • Humans
  • Italy
  • Male
  • Mutation*
  • RNA Splicing / genetics
  • RNA, Messenger / genetics

Substances

  • RNA, Messenger