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Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
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Brugada Syndrome in Spinal and Bulbar Muscular Atrophy
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Oculopharyngeal Muscular Dystrophy in Hispanic New Mexicans
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Molecular Basis of the Neurodegenerative Disorders
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Few Psychological Consequences of Presymptomatic Testing for Huntington Disease
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Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
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A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
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Trinucleotide Repeat Expansion in Neurological Disease
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Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
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