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Spinocerebellar Ataxia 10

Known as: SCA10 
National Institutes of Health

Related topics

Related topics

22 relations
ATXN10 geneAbnormal coordinationAbnormal pyramidal signsAbnormality of extrapyramidal motor function

Broader (3)

Ataxia, SpinocerebellarDNA Repeat ExpansionGenes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Ataxia espinocerebelar tipo 10 (SCA10) : evidências moleculares de um efeito fundador da mutação
Review
2014
Review
2014
[Advances in repeat-primed PCR assay for the genetic diagnosis of dynamic mutation diseases with large pathogenic expansions].
Dynamic mutation diseases are genetic diseases caused by unstable repeat expansions in coding region or noncoding region. The… 
2014
2014
Análise de haplótipos do gene ATXN10 em pacientes com ataxia espinocerebelar tipo 10 (SCA10)
2012
2012
Table 1. [Summary of Molecular Genetic Testing Used in SCA10].
2012
2012
Characterization of Sequence Interruptions in ATTCT Repeat Expansions in SCA10 (P05.027)
2010
2010
Avaliação de alelos mutantes no gene ATXN10 e identificação de pacientes com ataxia espinocerebelar do tipo 10 (SCA10)
2006
2006
A mechanism for SCA10 neurodegeneration due to intronic repeat expansion