Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function (2007)

Author(s): Davies VJ, Hollins AJ, Piechota MJ, Yip W, Davies JR, White KE, Nichols PP, Boulton ME, Votruba M

      • Journal: Human Molecular Genetics
      • Volume: 16
      • Issue: 11
      • Pages: 1307-1318
      • Publisher: Oxford University Press
      • Publication type: Article
      • Bibliographic status: Published