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Trinucleotide expansions in the SCA7 gene in a large family with spinocerebellar ataxia and craniocervical dystonia

✍ Scribed by Yan Lin; Jia-Yong Zheng; Yan-Hui Jin; Yan-Chen Xie; Zi-Bing Jin


Book ID
116770193
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
554 KB
Volume
434
Category
Article
ISSN
0304-3940

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## Abstract The cerebellar variant of multiple system atrophy (MSA‐C) has overlapping clinical features with the hereditary spinocerebellar ataxias (SCAs), but can usually be distinguished on a clinical basis. We describe a patient who developed a sporadic, late‐onset, rapidly progressive neurodege