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- W2166664098 endingPage "402" @default.
- W2166664098 startingPage "389" @default.
- W2166664098 abstract "The human mitochondrial genome is extremely small compared with the nuclear genome, and mitochondrial genetics presents unique clinical and experimental challenges. Despite the diminutive size of the mitochondrial genome, mitochondrial DNA (mtDNA) mutations are an important cause of inherited disease. Recent years have witnessed considerable progress in understanding basic mitochondrial genetics and the relationship between inherited mutations and disease phenotypes, and in identifying acquired mtDNA mutations in both ageing and cancer. However, many challenges remain, including the prevention and treatment of these diseases. This review explores the advances that have been made and the areas in which future progress is likely." @default.
- W2166664098 created "2016-06-24" @default.
- W2166664098 creator A5018057407 @default.
- W2166664098 creator A5081713869 @default.
- W2166664098 date "2005-05-01" @default.
- W2166664098 modified "2023-10-14" @default.
- W2166664098 title "Mitochondrial DNA mutations in human disease" @default.
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