Rare mutation in ELOVL4 gene in SCA34 and cognitive affection: Expounding the role of cerebellum

Clin Neurol Neurosurg. 2021 Nov:210:106983. doi: 10.1016/j.clineuro.2021.106983. Epub 2021 Oct 11.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Cerebellum / diagnostic imaging*
  • Cognition Disorders / diagnostic imaging*
  • Cognition Disorders / genetics*
  • Eye Proteins / genetics*
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Mutation / genetics
  • Spinocerebellar Ataxias / diagnostic imaging*
  • Spinocerebellar Ataxias / genetics*

Substances

  • ELOVL4 protein, human
  • Eye Proteins
  • Membrane Proteins