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Ataxia
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Genetic Markers
Most Correlated Genes
Most Correlated SNPs
MSTO1
SARS
NKX6-2
FGF14
TDP1
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
CEBPB_01
GSE14769_UNSTIM_VS_360MIN_LPS_BMDM_UP
CHOP_01
HALLMARK_UV_RESPONSE_UP
GSE7768_OVA_WITH_LPS_VS_OVA_WITH_MPL_IMMUNIZED_MOUSE_WHOLE_SPLEEN_6H_DN
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Curated Studies
Most Correlated Studies
Mouse Phenotypes - Degenerative disease of the CNS
Mouse Phenotypes - Autosomal recessive hereditary disorder
Mouse Phenotypes - Autosomal dominant hereditary disorder
Cerebellum and forbrain from ataxin-1 mutant mice
Frataxin deficiency in a Friedreich Ataxia mouse model is corrected by HDAC inhibitor
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Literature
Most Relevant Literature
Atypical retinopathy in ataxia with vitamin E deficiency: report of a sibship.
Stage-Dependent Biomarker Changes in Spinocerebellar Ataxia Type 3.
Paroxysmal dysarthria-ataxia syndrome.
A Milestone in the Treatment of Ataxias: Approval of Omaveloxolone for Friedreich Ataxia.
The episodic ataxias.
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Clinical Trials
Most Relevant Clinical Trials
Biomarkers in Friedreich's Ataxia
A Study on Cerebello-Spinal tPCS in Ataxia
Functional and Structural Imaging and Motor Control in Spinocerebellar Ataxia
4-Aminopyridine in Episodic Ataxia Type 2
Cerebellar Non-invasive Stimulation in Ataxias
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