Missense mutations of ACTA1 cause dominant congenital myopathy with cores

Research output: Contribution to journal › Research article › Contributed › peer-review

Contributors

  • Angela M. Kaindl - , Charité – Universitätsmedizin Berlin, Department of Child and Adolescent Psychiatry and Psychotherapy (Author)
  • F. Rüschendorf - , Max Delbrück Center for Molecular Medicine (MDC) (Author)
  • S. Krause - , Ludwig Maximilian University of Munich (Author)
  • H. H. Goebel - , Johannes Gutenberg University Mainz (Author)
  • K. Koehler - , Department of Paediatrics (Author)
  • C. Becker - , Max Delbrück Center for Molecular Medicine (MDC) (Author)
  • D. Pongratz - , Ludwig Maximilian University of Munich (Author)
  • J. Müller-Höcker - , Ludwig Maximilian University of Munich (Author)
  • P. Nürnberg - , Charité – Universitätsmedizin Berlin, Max Delbrück Center for Molecular Medicine (MDC) (Author)
  • G. Stoltenburg-Didinger - , Charité – Universitätsmedizin Berlin (Author)
  • H. Lochmüller - , Ludwig Maximilian University of Munich (Author)
  • A. Huebner - , Department of Paediatrics (Author)

Details

Original languageEnglish
Pages (from-to)842-848
Number of pages7
JournalJournal of medical genetics
Volume41
Issue number11
Publication statusPublished - Nov 2004
Peer-reviewedYes

External IDs

PubMed 15520409

Keywords

ASJC Scopus subject areas