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DYSTONIA 24

Known as: DYT24 
 
National Institutes of Health

Papers overview

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2019
2019
Background: Dystonia-24 (DYT24) is a monogenic autosomal dominant dystonia caused by mutations in the gene ANO3, which has shown… Expand
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2018
2018
Dear Editor, Mutations of ANO3 have recently been found to cause isolated dystonia (DYT24, MIM 615034), predominantly involving… Expand
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Review
2016
Review
2016
PURPOSE OF REVIEW This article highlights the clinical and diagnostic tools used to assess and classify dystonia and provides an… Expand
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2016
2016
BackgroundCervical dystonias have a variable presentation and underlying etiology, but collectively represent the most common… Expand
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2015
2015
  • Kishore R. Kumar
  • Movement disorders : official journal of the…
  • 2015
  • Corpus ID: 44822155
The advent of next-generation sequencing (NGS) has resulted in an expansion in the number of dystonia-causing genes identified… Expand
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2014
2014
Genes causing primary dystonia are rare. Recently, pathogenic mutations in the anoctamin 3 gene (ANO3) have been identified to… Expand
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Review
2014
Review
2014
Dystonia, a common and genetically heterogeneous neurological disorder, was recently defined as “a movement disorder… Expand
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Review
2013
Review
2013
Although all forms of dystonia share the core clinical features of involuntary dystonic dyskinesia, there is not only marked… Expand
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