STUB1-Related Ataxias: A Challenging Diagnosis: Movement Disorders Clinical Practice

S. Cocozza, F.M. Santorelli, G. De Michele

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)733-734
Number of pages2
JournalMov. Disord. Clin. Pract.
Volume7
Issue number6
DOIs
Publication statusPublished - 2020

Keywords

  • ataxia
  • dystonia
  • SCA48
  • SCAR16
  • STUB1
  • adult
  • case report
  • cerebellar peduncle
  • cerebellum atrophy
  • clinical article
  • female
  • gene
  • gene mutation
  • genetic counseling
  • genetic variability
  • human
  • Letter
  • middle aged
  • nerve conduction
  • phenotype
  • priority journal
  • spinocerebellar degeneration
  • STIP1 gene

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