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Oxford University Press

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Oxford University Press

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Mapping of the second Friedreich's ataxia () locus to chromosome 9p23-p11: evidence for further locus heterogeneity

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The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates

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Basal ganglia involvement of a patient with SCA 17: A new form of autosomal dominant spinocerebellar ataxia

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