1024C > T (R342X) is a recurrent PHF6 mutation also found in the original Borjeson-Forssman-Lehmann syndrome family

Research output: Contribution to journalLetter

Details

Authors
  • KM Lower
  • G Solders
  • ML Bondeson
  • J Nelson
  • Arne Brun
  • J Crawford
  • G Malm
  • M Borjeson
  • G Turner
  • M Partington
  • J Gecz
Organisations
Research areas and keywords

Subject classification (UKÄ) – MANDATORY

  • Medical Genetics
Original languageEnglish
Pages (from-to)787-789
JournalEuropean Journal of Human Genetics
Volume12
Issue number10
Publication statusPublished - 2004
Publication categoryResearch
Peer-reviewedNo

Bibliographic note

The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Pathology, (Lund) (013030000)