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2. Characteristic microglial features in patients with hereditary diffuse leukoencephalopathy with spheroids caused by mutations of the gene encoding the colony stimulating factor-1 receptor

4. Clinical features and natural history of pathologically confirmed corticobasal degeneration-Japanese multicenter validation study of CBD-

5. LMNB1-related adult-onset autosomal dominant leukodystrophy: Genetic and clinical studies of four Japanese families

19. Close Associations between Prevalences of Dominantly Inherited Spinocerebellar Ataxias with CAG-Repeat Expansions and Frequencies of Large Normal CAG Alleles in Japanese and Caucasian Populations

22. Japanese Families with Autosomal Dominant Pure Cerebellar Ataxia Map to Chromosome 19p13.1-p13.2 and Are Strongly Associated with Mild CAG Expansions in the Spinocerebellar Ataxia Type 6 Gene in Chromosome 19p13.1

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