Origin of mutation in sporadic cases of severe haemophilia A in Sweden.

Research output: Contribution to journalArticle

Abstract

Many newly diagnosed Swedish severe haemophilia A (HA) patients are sporadic cases. Some genotypically non-carrier mothers have gone on to have two descendants with the same mutation, presumably due to mosaicism.

Details

Authors
Organisations
External organisations
  • Kristianstad University
Research areas and keywords

Subject classification (UKÄ) – MANDATORY

  • Hematology
Original languageEnglish
Pages (from-to)63-68
JournalClinical Genetics
Volume90
Issue number1
Publication statusPublished - 2016
Publication categoryResearch
Peer-reviewedYes