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126,127 Familial genetic mutations and polymorphisms can also alter astrocyte functions in ways that contribute to disorder progression as noted in Huntingtons disease, 117,128 familial amyotrophic lateral sclerosis (ALS) mutations, 129,130 or familial AD mutations

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They may: Promote lipolysis (fat breakdown) Increase metabolic efficiency Improve mitochondrial function 4

it acts as a stable source of cysteine, which is necessary for glutathione synthesis

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