Browse by author
Lookup NU author(s): Professor Bobby McFarland,
Emeritus Professor Doug Turnbull
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
In 1998, Wallace et al. (Science 1988; 242: 1427-30) published evidence that the mutation m.11778G > A was responsible for causing Leber's hereditary optic neuropathy. This was the first account of a mitochondrial DNA mutation being irrefutably linked with a human disease and was swiftly followed by a report from Holt et al. (Nature 1988; 331: 717-9) identifying deletions in mitochondrial DNA as a cause for myopathy. During the subsequent 20 years there has been an exponential growth in 'mitochondrial medicine', with clinical, biochemical and genetic characterizations of a wide range of mitochondrial diseases and evidence implicating mitochondria in a host of many other clinical conditions including ageing, neurodegenerative illness and cancer. In this review we shall focus on the diagnosis and management of mitochondrial diseases that lead directly or indirectly to disruption of the process of oxidative phosphorylation.
Author(s): McFarland R, Turnbull DM
Publication type: Review
Publication status: Published
Journal: Journal of Internal Medicine
ISSN (print): 0954-6820
ISSN (electronic): 1365-2796