Spinocerebellar Ataxia Type 13

About the Disease
Spinocerebellar Ataxia 13, also known as spinocerebellar ataxia type 13, is related to hereditary ataxia and autosomal dominant cerebellar ataxia, and has symptoms including abnormal pyramidal signs and gait ataxia. An important gene associated with Spinocerebellar Ataxia 13 is KCNC3 (Potassium Voltage-Gated Channel Subfamily C Member 3), and among its related pathways/superpathways are Transmission across Chemical Synapses and Potassium Channels. Affiliated tissues include spinal cord, cerebellum and eye, and related phenotypes are nystagmus and dysarthria

Common Targets
KCNC3

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