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The Autosomal Recessive Cerebellar Ataxias
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Dopa-Responsive Dystonia Revisited
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Genetic Aspects of Alzheimer Disease
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Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
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Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
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The Tuberous Sclerosis Complex
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Genetic Screening for a Single Common LRRK2 Mutation in Familial Parkinson's Disease
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New Players in the Genetics of Stroke
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Complete Genomic Screen in Parkinson Disease
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The Human Genome Project,Application in the Diagnosis and Treatment of Neurologic Diseases
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The Muscular Dystrophies
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Clinical Genetics in Neurological Disease
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