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• W2089019624 endingPage "193" @default.
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• W2089019624 abstract "The majority of primary mitochondrial disorders are due to nuclear gene mutations, not aberrations within the mitochondrial genome. The nervous system is frequently involved due to its high-energy demands. Many nonspecific neurologic symptoms may be present in mitochondrial disease; however, there are well-recognized red flags that should alert the clinician to the possibility of mitochondrial disease. There is an ever increasing number of nuclear gene mutations discovered that play a role in primary mitochondrial disease and its neurologic symptomatology. Neurologists need to be aware of the wide neurologic presentation, the red-flag symptoms, and the nuclear gene mutations involved in the pathophysiology of mitochondrial disease to diagnose and manage this patient population." @default.
• W2089019624 created "2016-06-24" @default.
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• W2089019624 date "2012-12-01" @default.
• W2089019624 modified "2023-09-23" @default.
• W2089019624 title "Update on Nuclear Mitochondrial Genes and Neurologic Disorders" @default.
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• W2089019624 doi "https://doi.org/10.1016/j.spen.2012.09.005" @default.
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