## Abstract We report a 67 years old female patient out of a multigenerational family with spinocerebellar ataxia type 2 (SCA2) with an unusually benign course of disease. Although all SCA2 gene carriers have by now developed the predominant gait ataxia and brainstem oculomotor dysfunction, the ind
β¦ LIBER β¦
Rare association of motor neuron disease and spinocerebellar ataxia type 2 (SCA2): a new case and review of the literature
β Scribed by Lorenzo Nanetti; Roberto Fancellu; Chiara Tomasello; Cinzia Gellera; Davide Pareyson; Caterina Mariotti
- Publisher
- Springer
- Year
- 2009
- Tongue
- English
- Weight
- 117 KB
- Volume
- 256
- Category
- Article
- ISSN
- 0340-5354
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