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SPINOCEREBELLAR ATAXIA 11

Known as: SCA11 
National Institutes of Health

Related topics

Related topics

6 relations

Broader (1)

Ataxia, Spinocerebellar
Autosomal dominant inheritanceCerebellar atrophyDysarthriaNystagmus

Papers overview

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2011
2011
Mutations in the PDYN gene (SCA23) are not a frequent cause of dominant ataxia in Central Europe
To the Editor : Autosomal-dominant spinocerebellar ataxia (SCA) is a clinically and genetically heterogeneous neurodegenerative… 
Review
2009
Review
2009
[Molecular genetic approach to spinocerebellar ataxias].
Spinocerebellar ataxia (SCA) is a group of degenerative ataxias with autosomal dominant inheritance. The most common form of… 
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