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- W2046654387 abstract "Human mitochondrial diseases have been associated recently with mitochondrial DNA mutations, duplications and deletions which impair the protein synthesis of the mitochondrial subunits of the respiratory chain complexes. A constant feature is the coincident presence of the mutated and wild type genomes which provide heteroplasmy. The clinical expression of these diseases depends on the relative expression of each kind of mitochondrial DNA in the various tissues, which in turn affects the production of ATP in these tissues. Research on nuclear gene products interfering with mtDNA or with its gene products is the next step towards understanding the etiology of these diseases." @default.
- W2046654387 created "2016-06-24" @default.
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- W2046654387 date "1992-02-01" @default.
- W2046654387 modified "2023-09-27" @default.
- W2046654387 title "Mitochondrial DNA mutations in human diseases: a review" @default.
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- W2046654387 doi "https://doi.org/10.1016/0300-9084(92)90035-d" @default.
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