Spinocerebellar ataxia 22

Known as: SCA22 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2003-2014
012320032014

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
 
Is this relevant?
2013
2013
The autosomal dominant cerebellar ataxias (SCAs) are progressive neurodegenerative disorders caused by atrophy of the cerebellum… (More)
  • figure 1
Is this relevant?
2012
2012
OBJECTIVE To identify the causative gene in spinocerebellar ataxia (SCA) 22, an autosomal dominant cerebellar ataxia mapped to… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
Review
2012
Review
2012
I n this issue of Annals of Neurology, Duarri et al 1 and Lee et al 2 report the identification of a gene that when mutated… (More)
Is this relevant?
Review
2012
Review
2012
The spinocerebellar ataxias (SCAs) are a clinically and genetically heterogeneous group of dominantly inherited degenerative… (More)
Is this relevant?
Review
2005
Review
2005
The SCA19 locus on chromosome 1p21-q21 was identified in a Dutch family in 2002. Affected individuals displayed a lateonset… (More)
Is this relevant?
2004
2004
T he recent barrage of linkage assignments and gene discoveries has confirmed the clinical and genetic heterogeneity of ataxic… (More)
  • table 1
  • figure 1
  • figure 2
  • table 2
Is this relevant?
2003
2003
The autosomal dominant cerebellar ataxias (ADCA) are a clinically, pathologically and genetically heterogeneous group of… (More)
Is this relevant?