Splice site mutation in factor X gene manifesting as severe intracranial haemorrhage in neonatal period with a challenging treatment course

Haemophilia. 2017 Mar;23(2):e138-e140. doi: 10.1111/hae.13138. Epub 2016 Dec 19.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Base Sequence
  • Factor X / genetics*
  • Female
  • Humans
  • Infant, Newborn
  • Intracranial Hemorrhages / complications*
  • Intracranial Hemorrhages / genetics
  • Intracranial Hemorrhages / therapy*
  • Male
  • Mutation*
  • Pedigree
  • RNA Splice Sites / genetics*

Substances

  • RNA Splice Sites
  • Factor X