Publication:

An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy (1999)

Author(s): Clark KM, Taylor RW, Johnson MA, Chinnery PF, Chrzanowska-Lightowlers ZMA, Andrews RM, Nelson IP, Wood NW, Lamont PJ, Hanna MG, Lightowlers RN, Turnbull DM

      • Journal: American Journal of Human Genetics
      • Volume: 64
      • Issue: 5
      • Pages: 1330-1339
      • Publisher: Cell Press
      • Publication type: Article
      • Bibliographic status: Published
      Staff

      Professor Patrick Chinnery
      Wellcome Senior Fellow in Clinical Science, Professor of Neurogenetics and Honorary Consultant

      Professor Zofia Chrzanowska-Lightowlers
      Professor of Mitochondrial Biology

      Professor Robert Lightowlers
      Director, ICaMB and Professor of Molecular Neuroscience

      Professor Robert Taylor
      Professor of Mitochondrial Pathology