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Mitochondrial and redox modifications in early stages of Huntington’s disease

2022-01-15

Abstract excerpt

<h4>ABSTRACT</h4> Defects in mitochondrial function and mitochondrial-related redox deregulation have been attributed to Huntington’s disease (HD), a genetic neurodegenerative disorder largely affecting the striatum. However, whether these changes occur in early stages of the disease and can be detected in vivo is still unclear. Thus, in the present study, we analyzed changes in mitochondrial function and overre...

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Literature Corpus work
2247adc6-8951-55b8-a109-08323a1a6703
DOI
10.1101/2022.01.14.476381
Open publication

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Mitochondrial and redox modifications in early stages of Huntington’s diseaseDOI 10.1101/2022.01.14.476381
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