Article
Mitochondrial DNA mutations in disease, aging, and neurodegeneration.
Annals of the New York Academy of Sciences - 1 Dec 2008
Reeve Amy K, Krishnan Kim J, Turnbull Doug
Abstract excerpt
Patients with disorders from mutations in the mitochondrial genome have variable phenotypes, but common to many of these disorders are underlying changes in postmitotic cells, particularly neurons and muscle fibers. The mitochondrial dysfunction caused by these mutations has been shown to be associated with signs of apoptosis and to cause cell loss. Mutations of the mitochondrial genome have also been shown to...
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