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Spinocerebellar ataxia 36

Known as: SCA36 
National Institutes of Health

Related topics

Related topics

8 relations
Abnormal coordinationAutosomal dominant inheritanceCerebellar AtaxiaCerebellar atrophy

Papers overview

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2018
2018
Origen mutacional y expresión diferencial en SCA36
la ataxia espinocerebelosa tipo 36 o SCA36 es causada por expansion del hexanucleotido (GGCCTG)n localizado en el intron 1 de… 
2017
2017
Clinical characteristics of a novel ALS/SCA crossroad mutation Asidan (SCA36) (P2.210)
Objective: In oder to clarify clinical characteristics of a novel ALS/SCA crossroad muation Asidan (SCA36). Background: A novel… 
2017
2017
Clinical characteristics and detailed haplotype analysis of patients with SCA36 in Japan
2015
2015
Genetics of Dominant Ataxias
Dominant ataxias represent a clinically and genetically heterogeneous group of hereditary disorders comprising autosomal dominant… 
Review
2015
Review
2015
[Recent advances in clinical and genetic research of spinocerebellar ataxia type 36].
Non-coding expansion spinocerebellar ataxias (SCAs) are a group of autosomal dominant neurodegenerative diseases characterized by… 
2013
2013
Oromandibular dystonia associated with SCA36
examination showed homovanillic acid 73 nmol/L (reference values (r.v.) 148–434), 5-hydroxyindoleacetic acid 29 nmol/ L (r.v. 68… 
2013
2013
Clinical Features and Molecular Pathogenesis of Asidan/SCA36: A Novel Spinocerebellar Ataxia with Motor Neuron Involvement (P05.049)
OBJECTIVE: To characterize the phenotype and clarify the pathogenesis of spinocerebellar ataxia type 36 (SCA36), a novel dominant… 
2012
2012
GGCCTG repeats put a hex on Purkinje cells and motor neurons in SCA36
An increasing number of neurologic disorders are caused by microsatellite, or simple sequence, repeat expansions.[1][1] A group… 
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