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124,125 Another example of genetic primary astrocytopathy is the Duchenne muscular dystrophy (DMD) caused by mutations in the gene encoding dystrophin, which in the CNS is present almost exclusively in astrocytes

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The through-line: the more direct and higher-dose the form, the more the "who's dosing this and supervising it" question matters

The Carnitine Shuttle: Moving long-chain fatty acids in the mitochondria The carnitine shuttle is a three-step transport system that enables long-chain fatty acids to cross the inner mitochondrial membrane for -oxidation