Spinocerebellar Ataxia 10

Known as: Sca10 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1999-2017
0519992017

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2015
2015
Spino-cerebellar ataxia type 10 (SCA10) is an autosomal dominant disorder that is characterized by cerebellar ataxia, seizures… (More)
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2013
2013
This study describes the frequency of spinocerebellar ataxias and of CAG repeats range in different geographical regions of… (More)
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2009
2009
Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant neurodegenerative disorder characterized by ataxia and cerebellar… (More)
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2006
2006
BACKGROUND Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant disorder characterized by cerebellar ataxia and… (More)
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2006
2006
Spinocerebellar ataxia type 10 (SCA10) is one of numerous genetic disorders that result from simple repeat expansions. SCA10 is… (More)
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2004
2004
Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant ataxia caused by an ATTCT repeat expansion in an intron of the… (More)
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2004
2004
BACKGROUND Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive… (More)
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2003
2003
The autosomal dominant cerebellar ataxias (ADCA) are a clinically, pathologically and genetically heterogeneous group of… (More)
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2001
2001
Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant disorder caused by expansion of an unstable ATTCT repeat. SCA10… (More)
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Highly Cited
2000
Highly Cited
2000
Spinocerebellar ataxia type 10 (SCA10; MIM 603516; refs 1,2) is an autosomal dominant disorder characterized by cerebellar ataxia… (More)
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