Spinocerebellar Ataxia Type 6 (disorder)

Known as: SPINOCEREBELLAR ATAXIA 6, Spinocerebellar Ataxia-6, Spinocerebellar Ataxia 6s 
 
National Institutes of Health

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Highly Cited
2010
Highly Cited
2010
BACKGROUND AND OBJECTIVE Biomarkers to monitor neurological dysfunction in autosomal dominant inherited spinocerebellar ataxias… (More)
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2008
2008
OBJECTIVE The aim of this study was to evaluate cognitive impairment in patients with spinocerebellar ataxia type 6 (SCA6) and to… (More)
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Highly Cited
2008
Highly Cited
2008
OBJECTIVE To identify factors that determine disease severity and clinical phenotype of the most common spinocerebellar ataxias… (More)
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Highly Cited
2008
Highly Cited
2008
Spinocerebellar ataxia type 6 (SCA6) is a neurodegenerative disorder caused by CAG repeat expansions within the voltage-gated… (More)
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2004
2004
We performed a population-based clinical and molecular genetic study of spinocerebellar ataxia type 6 (SCA6) in the northeast of… (More)
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Review
2001
Review
2001
Spinocerebellar ataxia type 6 (SCA6) is due to small expansions of a CAG repeat at the 3' end of the CACNA1A gene, coding for the… (More)
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Highly Cited
1999
Highly Cited
1999
Spinocerebellar ataxia type 6 (SCA6) is one of the eight neurodegenerative diseases caused by a tri-nucleotide (CAG) repeat… (More)
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Highly Cited
1997
Highly Cited
1997
A polymorphic CAG repeat was identified in the human α1A voltage-dependent calcium channel subunit. To test the hypothesis that… (More)
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Highly Cited
1997
Highly Cited
1997
Spinocerebellar ataxia type 6 (SCA6) was recently identified as a form of autosomal dominant cerebellar ataxia associated with… (More)
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Highly Cited
1997
Highly Cited
1997
Point mutations of the CACNA1A gene coding for the alpha 1A voltage-dependent calcium channel subunit are responsible for… (More)
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