Spinocerebellar Ataxia Type 17

About the Disease
Spinocerebellar Ataxia 17, also known as spinocerebellar ataxia type 17, is related to spinocerebellar ataxia, autosomal recessive 17 and hereditary late-onset parkinson disease, and has symptoms including myoclonus, seizures and bradykinesia. An important gene associated with Spinocerebellar Ataxia 17 is TBP (TATA-Box Binding Protein), and among its related pathways/superpathways is Akt Signaling. Affiliated tissues include spinal cord, cerebellum and eye, and related phenotypes are ataxia and gait disturbance

Common Targets
TBP | CWF19L1 | STUB1

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