Phenotype variability in spinocerebellar
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Sascha Hering; Clemens AchmΓΌller; Andrea KΓΆhler; Werner Poewe; Raine Schneider;
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Article
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2009
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John Wiley and Sons
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English
β 457 KB
## 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