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Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6

✍ Scribed by Tezenas du Montcel, S.; Durr, A.; Rakowicz, M.; Nanetti, L.; Charles, P.; Sulek, A.; Mariotti, C.; Rola, R.; Schols, L.; Bauer, P.; Dufaure-Gare, I.; Jacobi, H.; Forlani, S.; Schmitz-Hubsch, T.; Filla, A.; Timmann, D.; van de Warrenburg, B. P.; Marelli, C.; Kang, J.-S.; Giunti, P.; Cook, A.; Baliko, L.; Bela, M.; Boesch, S.; Szymanski, S.; Berciano, J.; Infante, J.; Buerk, K.; Masciullo, M.; Di Fabio, R.; Depondt, C.; Ratka, S.; Stevanin, G.; Klockgether, T.; Brice, A.; Golmard, J.-L.

Book ID
121834582
Publisher
BMJ Publishing Group
Year
2014
Tongue
English
Weight
811 KB
Volume
51
Category
Article
ISSN
0022-2593

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Early symptoms in spinocerebellar ataxia
Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6
✍ Christoph Globas; Sophie Tezenas du Montcel; Laslo Baliko; Syliva Boesch; Chanta πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 159 KB

## 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