Spinocerebellar ataxia type 41 (SCA41)

Evidence-based neurology checklist on spinocerebellar ataxia type 41 (sca41): Genetics This is likely caused by mutations in the TRPC3 gene on chromosome 4q The transmission is autosomal dominant Clinical features Investigations

Genetics

  • This is likely caused by mutations in the TRPC3 gene on chromosome 4q
  • The transmission is autosomal dominant

Clinical features

Investigations

References

  1. Fogel BL, Hanson SM, Becker EB. Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans? Mov Disord 2015; 30:284-286.
  2. Becker EB, Fogel BL, Rajakulendran S, et al. Candidate screening of the TRPC3 gene in cerebellar ataxia. Cerebellum 2011; 10:296-299.

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