Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency

Research output: Contribution to journalJournal articleResearchpeer-review

  • P.S. Andersen
  • O. Havndrup
  • H. Bundgaard
  • Larsen, Lars Allan
  • J. Vuust
  • A.K. Pedersen
  • K. Kjeldsen
  • M. Christiansen
Original languageEnglish
JournalEuropean Journal of Human Genetics
Issue numberVol. 12
Pages (from-to)673-677
ISSN1018-4813
Publication statusPublished - 2004

ID: 104065