Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: A novel disorder of mtDNA maintenance (2008)

Author(s): Hudson G, Amati-Bonneau P, Blakely E, Stewart J, He L, Schaefer A, Griffiths P, Ahlqvist K, Suomalainen A, Reynier P, McFarland R, Turnbull D, Chinnery P, Taylor R

      • Journal: Brain
      • Volume: 131
      • Issue: 2
      • Pages: 329-337
      • Publisher: Oxford University Press
      • Publication type: Article
      • Bibliographic status: Published

      Dr Gavin Hudson
      Research Fellow