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Spinocerebellar ataxia type 15

2012
Spinocerebellar ataxia type 15 (SCA15), first described in 2001, is a slowly progressive, relatively pure dominantly inherited ataxia. Six pedigrees have been reported to date, in Anglo-Celtic and Japanese populations. Other than notably slow progression, its main distinguishing characteristic is tremor, often affecting the head, which is seen in about
Elsdon, Storey, R J McKinlay, Gardner
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Spinocerebellar ataxia type 10

2012
Clinical characteristics Spinocerebellar ataxia type 10 (SCA10) is characterized by slowly progressive cerebellar ataxia that usually starts as poor balance and unsteady gait, followed by upper-limb ataxia, scanning dysarthria, and dysphagia. Abnormal tracking eye movements are common.
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Other spinocerebellar ataxias

2012
Leslie J, Cloud, George, Wilmot
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Spinocerebellar ataxia type 7

2012
Spinocerebellar ataxia type 7 (SCA7) is associated with progressive blindness, dominant transmission, and marked anticipation. SCA7 represents one of the polyglutamine expansion diseases with increase of CAG repeats. The gene maps to chromosome 3p12-p21.1. Normal values of CAG repeats range from 4 to 18.
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Spinocerebellar Ataxias

2009
Alexander K. C. Leung   +150 more
openaire   +1 more source

Polyglutamine spinocerebellar ataxias: emerging therapeutic targets

Expert Opinion on Therapeutic Targets, 2020
Andreia Carvalho   +2 more
exaly  

Spinocerebellar ataxias: prospects and challenges for therapy development

Nature Reviews Neurology, 2018
Tetsuo Ashizawa   +2 more
exaly  

Polyglutamine spinocerebellar ataxias — from genes to potential treatments

Nature Reviews Neuroscience, 2017
Henry L Paulson   +2 more
exaly  

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