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New Players in the Genetics of Stroke
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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The Clinical Spectrum of Familial Hemiplegic Migraine Associated with Mutations in a Neuronal Calcium Channel
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Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
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Reduced Basal Ganglia Volume Associated with the Gene for Huntington's Disease in Asymptomatic at-Risk Persons
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