Limb girdle muscular dystrophy type 2I caused by a novel missense mutation in the FKRP gene presenting as acute virus-associated myositis in infancy

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Maja Der Von Der Hagen - , Department of Paediatrics, Division of Neuropediatrics (Author)
  • Angela M. Kaindl - , Charité – Universitätsmedizin Berlin (Author)
  • Kathrin Koehler - , Department of Paediatrics, University Hospital Carl Gustav Carus Dresden (Author)
  • Petra Mitzscherling - , University Hospital Carl Gustav Carus Dresden, Department of Child and Adolescent Psychiatry and Psychotherapy (Author)
  • Hans Jürgen Häusler - , University Hospital Carl Gustav Carus Dresden, Department of Child and Adolescent Psychiatry and Psychotherapy (Author)
  • Gisela Stoltenburg-Didinger - , Charité – Universitätsmedizin Berlin (Author)
  • Angela Huebner - , Department of Paediatrics, University Hospital Carl Gustav Carus Dresden (Author)

Details

Original languageEnglish
Pages (from-to)62-63
Number of pages2
JournalEuropean journal of pediatrics
Volume165
Issue number1
Publication statusPublished - Jan 2006
Peer-reviewedYes

External IDs

PubMed 16143867

Keywords