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SPINOCEREBELLAR ATAXIA 23

Known as: SCA23 
 
National Institutes of Health

Papers overview

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2019
2019
Spinocerebellar Ataxia 23 (SCAR23) is a newly described condition caused by mutations in TDP2 gene. To date, only four patients… Expand
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2016
2016
Sir, We read with interest the recent publication by Smeets et al. (2015) on the generation of transgenic mouse for autosomal… Expand
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2015
2015
Advances in molecular genetics techniques have given several approaches to diagnose most common complex genetic disorders and… Expand
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2013
2013
We have recently identified missense mutations in prodynorphin (PDYN), the precursor to dynorphin opioid peptides, as the cause… Expand
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2013
2013
The autosomal dominant cerebellar ataxias (SCAs) are progressive neurodegenerative disorders caused by atrophy of the cerebellum… Expand
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2012
2012
Spinocerebellar ataxias (SCA) are a genetically heterogeneous group of neurodegenerative diseases characterised by progressive… Expand
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2011
2011
To the Editor : Autosomal-dominant spinocerebellar ataxia (SCA) is a clinically and genetically heterogeneous neurodegenerative… Expand
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Highly Cited
2010
Highly Cited
2010
Spinocerebellar ataxias (SCAs) are dominantly inherited neurodegenerative disorders characterized by progressive cerebellar… Expand
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Highly Cited
2004
Highly Cited
2004
We report upon a Dutch autosomal dominant cerebellar ataxia (ADCA) family, clinically characterized by a late-onset (>40 years… Expand
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2004
2004
We report upon a Dutch autosomal dominant cerebellar ataxia (ADCA) family, clinically characterized by a lateonset (>40 years… Expand
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