Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Michaela Jaksch - , Helmholtz Zentrum München - German Research Center for Environmental Health (Author)
  • Claudia Paret - (Author)
  • Rolf Stucka - , Ludwig Maximilian University of Munich (Author)
  • Nina Horn - , JFK Institute Glostrup (Author)
  • Josef Müller-Höcker - , Ludwig Maximilian University of Munich (Author)
  • Rita Horvath - , Helmholtz Zentrum München - German Research Center for Environmental Health (Author)
  • Nadine Trepesch - , Helmholtz Zentrum München - German Research Center for Environmental Health (Author)
  • Gerhard Stecker - , Helmholtz Zentrum München - German Research Center for Environmental Health (Author)
  • Peter Freisinger - , Haunersches Kinderspital in Munich (Author)
  • Christian Thirion - , Ludwig Maximilian University of Munich (Author)
  • Juliane Müller - , Ludwig Maximilian University of Munich (Author)
  • Renate Lunkwitz - , TUD Dresden University of Technology (Author)
  • Gerhard Rödel - , Chair of General Genetics (Author)
  • Eric A. Shoubridge - , McGill University (Author)
  • Hanns Lochmüller - , Ludwig Maximilian University of Munich (Author)

Details

Original languageEnglish
Pages (from-to)3025-3035
JournalHuman Molecular Genetics
Volume10
Publication statusPublished - 2001
Peer-reviewedYes

External IDs

Scopus 0035894664

Keywords