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Rare association of motor neuron disease and spinocerebellar ataxia type 2 (SCA2): a new case and review of the literature

✍ 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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## 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

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