Journal of Neurology

, Volume 260, Issue 7, pp 1931–1933

Autosomal dominant mutations in POLG and C10orf2: association with late onset chronic progressive external ophthalmoplegia and Parkinsonism in two patients

Authors

  • Barton R. Brandon
    • Rush University Medical Center
  • Nico J. Diederich
    • Centre Hospitalier de Luxembourg and Luxembourg Center for Systems Biomedicine
  • Madhu Soni
    • Rush University Medical Center
  • Katrin Witte
    • Mitochondrial Disease Group, Department of NeurologyUniklinikum CG Carus, TU Dresden
  • Manja Weinhold
    • Mitochondrial Disease Group, Department of NeurologyUniklinikum CG Carus, TU Dresden
  • Micaela Krause
    • Mitochondrial Disease Group, Department of NeurologyUniklinikum CG Carus, TU Dresden
    • Mitochondrial Disease Group, Department of NeurologyUniklinikum CG Carus, TU Dresden
Letter to the Editors

DOI: 10.1007/s00415-013-6975-2

Cite this article as:
Brandon, B.R., Diederich, N.J., Soni, M. et al. J Neurol (2013) 260: 1931. doi:10.1007/s00415-013-6975-2

Copyright information

© Springer-Verlag Berlin Heidelberg 2013