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SPINOCEREBELLAR ATAXIA 38

Known as: SCA38 
National Institutes of Health

Related topics

Related topics

8 relations
Autosomal dominant inheritanceCerebellar AtaxiaCerebellar atrophyDysarthria

Papers overview

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2020
2020
Docosahexaenoic acid in ARSACS: observations in two patients
Background Spastic ataxia of Charlevoix-Saguenay is a neurodegenerative condition due to mutations in the SACS gene and without a… 
2015
2015
SCA38 is rare in mainland China
2015
2015
Unraveling molecular pathogenesis of SCA38, a novel autosomal dominant ataxia with a possible treatment
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