Neurology · 2006 · 23 citations · 4 references
Life SciencesNeurologyNeuroscienceDiagnostic RadiologyMitochondrial BiologyNeuropathologyMitochondrial DiseaseMitochondrial DisordersMitochondrial DysfunctionMitochondrial Neurological DisordersNeurodegenerative DiseasesNeurodegenerative DisordersMitochondrial Disease PathologyMitochondrial Dna Depletion SyndromesMitochondrial MyopathiesMitochondrial NeuropathologyNeuroimaging In Mitochondrial DisordersSkeletal MyopathySpongiform DegenerationStructural Mri
The authors studied seven patients with mitochondrial DNA (mtDNA) myopathy. Over time, there was a progressive depletion of mtDNA, which preferentially affected wild-type mitochondrial genomes. This suggests that loss of wild-type mtDNA is a major feature of mtDNA myopathy, and preventing wild-type mtDNA depletion has treatment implications.
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