Publication:

OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules (2010)

Author(s): Yu-Wai-Man P, Sitarz KS, Samuels DC, Griffiths PG, Reeve AK, Bindoff LA, Horvath R, Chinnery PF

      • Date: 18-05-2010
      • Journal: Human Molecular Genetics
      • Volume: 19
      • Issue: 15
      • Pages: 3043-3052
      • Publisher: Oxford University Press
      • Publication type: Article
      • Bibliographic status: Published

      Keywords: MITOCHONDRIAL TRANSCRIPTION FACTOR HUMAN SKELETAL-MUSCLE HEREDITARY OPTIC NEUROPATHIES DNA MUTATIONS FACTOR-A EXTERNAL OPHTHALMOPLEGIA NIGRA NEURONS APOPTOSIS DISEASE ATROPHY

      Staff

      Professor Patrick Chinnery
      Institute Director

      Dr Patrick Yu Wai Man
      MRC Clinician Scientist