## 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 ✦
Oxidative stress parameters in plasma of Huntington's disease patients, asymptomatic Huntington’s disease gene carriers and healthy subjects
✍ Scribed by N. Klepac; M. Relja; R. Klepac; S. Hećimović; T. Babić; V. Trkulja
- Publisher
- Springer
- Year
- 2007
- Tongue
- English
- Weight
- 309 KB
- Volume
- 254
- Category
- Article
- ISSN
- 0340-5354
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