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- W2774741628 abstract "Background: SCA36 is an autosomal-dominant neurodegenerative disorders caused by the expansion of a hexanucleotide GGCCTG repeat within intron1 of the nucleolar protein 56 gene. SCA36 presents a wide spectrum of neurodegeneration for extrapyramidal and autonomic systems, involving cerebellar, motor system and cognitive function." @default.
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- W2774741628 date "2017-10-01" @default.
- W2774741628 modified "2023-09-25" @default.
- W2774741628 title "Clinical characteristics of spinocerebellar ataxia type 36 (SCA36) in South Kyusyu, Japan" @default.
- W2774741628 doi "https://doi.org/10.1016/j.jns.2017.08.2506" @default.
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