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Olfactory Functions in Asymptomatic Carriers of the Huntington Disease Mutation

✍ Scribed by Larsson, Maria; Lundin, Anders; Robins Wahlin, Tarja-Brita


Book ID
127071447
Publisher
Taylor and Francis Group
Year
2006
Tongue
English
Weight
89 KB
Volume
28
Category
Article
ISSN
1380-3395

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## Abstract Huntington's disease (HD) is an autosomal dominantly inherited neurodegenerative disorder caused by a CAG repeat expansion in the __IT‐15__ gene; however, it remains unknown how the mutation leads to selective neurodegeneration. Several lines of evidence suggest impaired mitochondrial f