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Spinocerebellar ataxia types 1, 2, 3, and 6: Disease severity and nonataxia symptoms

✍ 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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## 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