Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation

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

  • N.K. Olsen
  • A.W. Hansen
  • Søren Nørby
  • A.L. Edal
  • J.R. Jørgensen
  • T. Rosenberg
Genetik, Leber's opticusatrofi, dissemineret sclerose, mitokondrie-DNA, mutation
Original languageEnglish
JournalActa Neurologica Scandinavica
Issue numberVol 91
Pages (from-to)326-329
ISSN0001-6314
Publication statusPublished - 1995

ID: 244701