Article
Renal disease and mitochondrial genetics.
Journal of nephrology - 1 Jan 2000
Rötig Agnès
Abstract excerpt
Respiratory chain (RC) deficiencies have long been regarded as neuromuscular diseases mainly originating from mutations in the mitochondrial DNA. Oxidative phosphorylation, i.e. adenosine triphosphate (ATP) synthesis-coupled electron transfer from substrate to oxygen through the RC, does not occu...
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