A novel SETX gene mutation producing ataxia with oculomotor apraxia type 2

Laszlo Szpisjak, Izabella Obal, J. Engelhardt, L. Vécsei, P. Klivényi

Research output: Contribution to journalArticle

1 Citation (Scopus)
Original languageEnglish
Pages (from-to)1-3
Number of pages3
JournalActa Neurologica Belgica
DOIs
Publication statusAccepted/In press - Jan 25 2016

Keywords

  • Ataxia with oculomotor apraxia type 2
  • Early-onset ataxia
  • Novel senataxin mutation

ASJC Scopus subject areas

  • Clinical Neurology

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