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Spinocerebellar ataxia type 15
2012Spinocerebellar 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
2012Clinical 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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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 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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Polyglutamine spinocerebellar ataxias: emerging therapeutic targets
Expert Opinion on Therapeutic Targets, 2020Andreia Carvalho +2 more
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Spinocerebellar ataxias: prospects and challenges for therapy development
Nature Reviews Neurology, 2018Tetsuo Ashizawa +2 more
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Polyglutamine spinocerebellar ataxias — from genes to potential treatments
Nature Reviews Neuroscience, 2017Henry L Paulson +2 more
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