Spinocerebellar Ataxia 37 (SCA37)

Spinocerebellar Ataxia 37, also known as spinocerebellar ataxia type 37, is related to autosomal dominant cerebellar ataxia and familial adult myoclonic epilepsy, and has symptoms including cerebellar ataxia An important gene associated with Spinocerebellar Ataxia 37 is DAB1 (DAB Adaptor Protein 1), and among its related pathways/superpathways are Guidance Cues and Growth Cone Motility and Reelin Pathway (Cajal-Retzius cells). Affiliated tissues include eye and spinal cord, and related phenotypes are cogwheel rigidity and falls