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ENSpinocerebellar Ataxia 31 (SCA31)
Alias:
Spinocerebellar Ataxia Type 31
Sca31
Pure Spinocerebellar Ataxia Japanese Type
Spinocerebellar Ataxia, 16q22-Linked
Spinocerebellar Ataxia 16q22-Linked
Ataxia, Spinocerebellar, Type 31
Sca4 Pure Japanese Type
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Spinocerebellar Ataxia 31, also known as spinocerebellar ataxia type 31, is related to spinocerebellar ataxia 1 and hereditary spastic paraplegia, and has symptoms including gait ataxia An important gene associated with Spinocerebellar Ataxia 31 is BEAN1 (Brain Expressed Associated With NEDD4 1). Affiliated tissues include spinal cord and cerebellum, and related phenotypes are dysarthria and gait ataxia
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