Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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Fragile X Premutation With Atypical Symptoms at Onset
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Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
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Molecular Basis of the Neurodegenerative Disorders
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The Inherited Ataxias and the New Genetics
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