Spinocerebellar Ataxia Type 21

About the Disease
Spinocerebellar Ataxia 21, also known as spinocerebellar ataxia type 21, is related to spinocerebellar ataxia, autosomal recessive 21 and hereditary ataxia, and has symptoms including cerebellar ataxia, tremor and cogwheel rigidity. An important gene associated with Spinocerebellar Ataxia 21 is TMEM240 (Transmembrane Protein 240). Affiliated tissues include spinal cord, cerebellum and eye, and related phenotypes are abnormality of extrapyramidal motor function and gait ataxia

Common Targets
SCYL1 | TMEM240

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