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The cortical silent period in normal subjects and in disease

✍ Scribed by A. Berardelli


Book ID
115869576
Publisher
Elsevier Science
Year
1993
Tongue
English
Weight
213 KB
Volume
87
Category
Article
ISSN
0013-4694

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## Abstract Spinocerebellar ataxia 6 (SCA6) is a hereditary disease characterized by a trinucleotide repeat expansion in the CACNA1A gene and late‐onset bilateral cerebellar atrophy. It is unclear if there is significant pathology outside of the cerebellum. We used transcranial magnetic stimulation