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Spinocerebellar ataxia 36

Known as: SCA36 
 
National Institutes of Health

Papers overview

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2020
2020
SCA36 is an autosomal dominant spinocerebellar ataxia (SCA) affecting many families from Costa da Morte, a northwestern region of… Expand
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2018
2018
BackgroundSpinocerebellar ataxia (SCA) subtypes are often caused by expansions in non-coding regions of genes like SCA8, SCA10… Expand
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2017
2017
BACKGROUND The spinocerebellar ataxias (SCAs) form a clinically, genetically, and pathological heterogeneous group of autosomal… Expand
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2017
2017
Resumen Introduccion-objetivos Describir la historia del descubrimiento de la SCA36 y revisar los conocimientos actuales sobre… Expand
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2017
2017
Objective: In oder to clarify clinical characteristics of a novel ALS/SCA crossroad muation Asidan (SCA36). Background: A novel… Expand
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2013
2013
BACKGROUND We report on a unique complication of cerebellar ataxia and motor neuron disease named Asidan/SCA36 with a high… Expand
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2013
2013
 
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2012
2012
BACKGROUND A variety of hereditary spinocerebellar ataxia (SCA) develops a broad spectrum of both ataxia and non-ataxia symptoms… Expand
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2012
2012
An increasing number of neurologic disorders are caused by microsatellite, or simple sequence, repeat expansions.1 A group of… Expand
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Highly Cited
2011
Highly Cited
2011
Autosomal-dominant spinocerebellar ataxias (SCAs) are a heterogeneous group of neurodegenerative disorders. In this study, we… Expand
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