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cerebellar ataxia
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
ATXN3
APTX
KCNA1
RORA
EXOSC5
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
cellular potassium ion transport
potassium ion transmembrane transport
neuromuscular process
response to mechanical stimulus
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Curated Studies
Most Correlated Studies
OMIM - CAPOS syndrome
Epithelial cells from kidney organoids of Mainzer-Saldino syndrome patient iPSC with IFT140 mutation
OMIM - Disorder of brain
OMIM - Developmental disorders
OMIM - Ataxia
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Literature
Most Relevant Literature
Gene Suppression Therapies in Hereditary Cerebellar Ataxias: A Systematic Review of Animal Studies.
Immune-Mediated Cerebellar Ataxias].
Autoimmune Cerebellar Ataxia: Etiology and Clinical Characteristics of a Case Series from China.
Cerebellar ataxia with anti-mGluR1 auto-antibody in a pediatric patient: A case report.
Anti-neurochondrin antibody as a biomarker in primary autoimmune cerebellar ataxia-a case report and…
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Clinical Trials
Most Relevant Clinical Trials
A Registered Cohort Study on Cerebellar Ataxia
Augmenting Balance in Individuals With Cerebellar Ataxias
Effect of Riluzole as a Symptomatic Approach in Patients With Chronic Cerebellar Ataxia
Efficacy of Riluzole in Hereditary Cerebellar Ataxia
Dual Task Training for Cerebellar Ataxia
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