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Late-Onset Friedreich Ataxia
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Oculopharyngeal Muscular Dystrophy in Hispanic New Mexicans
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Few Psychological Consequences of Presymptomatic Testing for Huntington Disease
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Phenotypic Variability in Friedreich Ataxia:Role of the Associated GAA Triplet Repeat Expansion
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Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
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Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
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Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
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Clinical Genetics in Neurological Disease
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Trinucleotide Repeat Expansion in Neurological Disease
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Molecular Genetics in Neurology
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