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- W331206944 abstract "Spinocerebellar ataxia type 7 (SCA7) is a hereditary neurodegenerative disorder affecting the cerebellum, pons and retina. SCA7 patients present with gait ataxia and visual impairment as the main s ..." @default.
- W331206944 created "2016-06-24" @default.
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- W331206944 date "2000-01-01" @default.
- W331206944 modified "2023-09-27" @default.
- W331206944 title "Genetic and Molecular analysis of the Spinocerebellar ataxia type 7 (SCA7) disease gene" @default.
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