Lookup NU author(s): Professor Mark Birch-Machin,
Professor Robert Taylor,
Professor Doug Turnbull
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
Genetic defects affecting the mitochondrial respiratory chain are an important cause of neurological disease. Previously, we identified a family with complex II deficiency and late-onset neurodegenerative disease with progressive optic atrophy, ataxia, and myopathy. The affected family members are now shown to carry a C-to-T transition in one allele of the nuclear gene encoding the flavoprotein subunit of complex II. Mutation of the equivalent base in Escherichia coli generates an inactive enzyme unable to bind flavin adenine dinucleotide covalendy. Compatible with these findings, our patients have an approximate 50% decrease in complex II and succinate dehydrogenase activity. These results suggest that genetic defects of nuclear-encoded subunits of the mitochondrial respiratory chain can result in late-onset neuro-degenerative disease.
Author(s): Taylor RW; Birch-Machin MA; Turnbull DM; Cochran B; Ackrell BAC
Publication type: Article
Publication status: Published
Journal: Annals of Neurology
Print publication date: 01/01/2000
ISSN (print): 0364-5134
ISSN (electronic): 1531-8249
Publisher: John Wiley & Sons
PubMed id: 10976639
Altmetrics provided by Altmetric