SPINOCEREBELLAR ATAXIA 18

Known as: SCA18, SMNA, Sensorimotor neuropathy with ataxia, autosomal dominant 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2002-2017
0120022017

Papers overview

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2017
2017
Spinocerebellar ataxias (SCAs) are a group of autosomal dominant, clinically heterogeneous neurodegenerative disorders. SCA18 is… (More)
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2014
2014
OBJECTIVE To explore the expression status of carbonic anhydrase III (CAIII) from quadriceps femoris muscle in two kinds of… (More)
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2009
2009
We have established strong linkage evidence that supports mapping autosomal-dominant sensory/motor neuropathy with ataxia (SMNA… (More)
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Review
2005
Review
2005
Spinocerebellar ataxias (SCAs) are a clinically heterogeneous group of disorders. Current molecular classification corresponds to… (More)
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2002
2002
The autosomal dominant (AD) spinocerebellar ataxias (SCAs) and hereditary sensory neuropathies (HSN) are heterogeneous disorders… (More)
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