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Spinocerebellar Ataxia Type 8
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Molecular Basis of the Neurodegenerative Disorders
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CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
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Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
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Calcium Channels in Neurological Disease
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Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
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The Inherited Ataxias and the New Genetics
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