Disease

Spinocerebellar Ataxia Type 42

About the Disease
Spinocerebellar Ataxia 42, also known as spinocerebellar ataxia type 42, is related to spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits and hereditary ataxia. An important gene associated with Spinocerebellar Ataxia 42 is CACNA1G (Calcium Voltage-Gated Channel Subunit Alpha1 G). Affiliated tissues include spinal cord, cerebellum and eye, and related phenotypes are dysarthria and unsteady gait

Common Targets
CACNA1G

疾病靶点研报
Spinocerebellar Ataxia Type 42

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