## Abstract Onset of genetically determined neurodegenerative diseases is difficult to specify because of their insidious and slowly progressive nature. This is especially true for spinocerebellar ataxia (SCA) because of varying affection of many parts of the nervous system and huge variability of
β¦ LIBER β¦
Spinocerebellar ataxia types 1, 2, 3, and 6: Disease severity and nonataxia symptoms
β Scribed by Schmitz-Hubsch, T.; Coudert, M.; Bauer, P.; Giunti, P.; Globas, C.; Baliko, L.; Filla, A.; Mariotti, C.; Rakowicz, M.; Charles, P.; Ribai, P.; Szymanski, S.; Infante, J.; van de Warrenburg, B.P.C.; Durr, A.; Timmann, D.; Boesch, S.; Fancellu, R.; Rola, R.; Depondt, C.; Schols, L.; Zdienicka, E.; Kang, J. -S.; Dohlinger, S.; Kremer, B.; Stephenson, D. A.; Melegh, B.; Pandolfo, M.; di Donato, S.; du Montcel, S. T.; Klockgether, T.
- Book ID
- 118266977
- Publisher
- Lippincott Williams and Wilkins
- Year
- 2008
- Tongue
- English
- Weight
- 409 KB
- Volume
- 71
- Category
- Article
- ISSN
- 0028-3878
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