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spinocerebellar ataxias 6
Summary
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Curated Studies
Most Correlated Studies
Lymphoblastoid cell lines of Spinocerebellar Ataxia Type 28 patients (mutated AFG3L2)
Cerebella from SCA6 MPI 118Q/118Q and MPI 11Q/11Q knockin spinocerebellar ataxia mouse models
ATM-dependent regulation of gene expression upon DNA damage in human fibroblasts
Medulloblastoma Daoy cells with ZBTB7B R363L and ZBTB7B wildtype overexpression
Early symptomatic Sca1154Q/2Q & Sca7266Q/5Q knockin cerebellum
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Literature
Most Relevant Literature
Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian…
Infantile onset spinocerebellar ataxia 2 (SCA2): a clinical report with review of previous cases.
Dopa-responsive dystonia in spinocerebellar ataxia 6: A case report.
Autosomal recessive spinocerebellar ataxia-20 due to a novel SNX14 variant in an Indian girl.
Small-expanded allele spinocerebellar ataxia 17: imaging and phenotypic variability.
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Clinical Trials
Most Relevant Clinical Trials
Parkinsonism in Spinocerebellar Ataxia Type 6
Dalfampridine and Gait in Spinocerebellar Ataxias
Study of CAD-1883 for Spinocerebellar Ataxia
Functional and Structural Imaging and Motor Control in Spinocerebellar Ataxia
Natural History Study of and Genetic Modifiers in Spinocerebellar Ataxias
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