## 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
✦ LIBER ✦
Cognitive changes in patients with Huntington’s disease (HD) and asymptomatic carriers of the HD mutation
✍ Scribed by J. Lemiere; M. Decruyenaere; G. Evers-Kiebooms; E. Vandenbussche; R. Dom
- Publisher
- Springer
- Year
- 2004
- Tongue
- English
- Weight
- 275 KB
- Volume
- 251
- Category
- Article
- ISSN
- 0340-5354
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