Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG gene

Lignende værker

• The first family case of spinocerebellar ataxia type 14 in Russia
  af: E. P. Nuzhnyy, et al.
  Udgivet: (2022-09-01)
• Writer's Cramp as the First Symptom of Spinocerebellar Ataxia 14
  af: Erro, Roberto, et al.
  Udgivet: (2014)
• Neurochemical Differences in Spinocerebellar Ataxia Type 14 and 1
  af: Grosch, Anne Sophie, et al.
  Udgivet: (2020)
• A family with spinocerebellar ataxia and retinitis pigmentosa attributed to an ELOVL4 mutation
  af: Xiao, Changrui, et al.
  Udgivet: (2019)
• Investigation of Visual System Involvement in Spinocerebellar Ataxia Type 14
  af: Ihl, Thomas, et al.
  Udgivet: (2020)