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1. Genetic and Molecular analysis of the Spinocerebellar ataxia type 7 (SCA7) disease gene
Sammanfattning : 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 symptoms. LÄS MER
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