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Published in 2019 at "Frontiers in Neurology"
DOI: 10.3389/fneur.2019.00453
Abstract: Huntington's disease (HD) is a rare, hereditary, neurodegenerative and dominantly transmitted disorder affecting about 10 out of 100,000 people in Western Countries. The genetic cause is a CAG repeat expansion in the huntingtin gene (HTT),…
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