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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Amyotrophic Lateral Sclerosis
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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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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Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene
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Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
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