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SPINOCEREBELLAR ATAXIA 8

Known as: SCA8 
National Institutes of Health

Papers overview

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2017
2017
Spinocerebellar ataxia types 1 (SCA1, OMIM# 164400) and 8 (SCA8, OMIM# 608768) are autosomal dominant, inherited ataxias. SCA1 is… 
2017
2017
Identification of Spoon as a suppressor of SCA8 associated neurodegeneration provides us a hint about its role in neuronal… 
2016
2016
Spinocerebellar degeneration (SCD) is a group of disorders characterized by progressive ataxia caused by dysfunction and atrophy… 
2005
2005
BACKGROUND Dominantly inherited spinocerebellar ataxia (SCA) is a clinically and genetically heterogeneous group of… 
2002
2002
The autosomal dominant spinocerebellar ataxias (SCAs) are a group of neurodegenerative diseases characterized by progressive… 
2002
2002
Since the original description of SCA8 in 1999,1 several reports have been published on the occurrence of the SCA8 gene CTG… 
Review
2000
Review
2000
Autosomal‐dominant cerebellar ataxias (ADCA) may present as progressive or paroxysmal disorders. While the progressive ataxias… 
1998
1998
Chromosome band 10q24 appears to be a gene-rich region, given the elevated number of expressed sequence tags (ESTs) already…