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- W2912366904 abstract "Mitochondrial myopathies belong to a group of diseases with defective oxidative phosphorylation. Mitochondrial myopathy is typically expressed as a myopathy with ragged red fibers and biochemical and/or histochemical evidence of oxidative phosphorylation deficiency. In oxidative phosphorylation diseases, the identification of a mitochondrial myopathy is frequently an important part of the diagnostic procedure. Clinical investigation, muscle pathology, and biochemical analysis of the oxidative phosphorylation function are important tools to direct the genetic analysis, which can involve mitochondrial DNA as well as nuclear DNA." @default.
- W2912366904 created "2019-02-21" @default.
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- W2912366904 date "2013-07-08" @default.
- W2912366904 modified "2023-10-14" @default.
- W2912366904 title "Mitochondrial Myopathies" @default.
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- W2912366904 doi "https://doi.org/10.1002/9781118635469.ch22" @default.
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