Atypical adult onset complicated spastic paraparesis with thin corpus callosum in two patients carrying a novel FA2H mutation

A. Tonelli, M. G. D'Angelo, F. Arrigoni, E. Brighina, A. Arnoldi, A. Citterio, N. Bresolin, M. T. Bassi

Research output: Contribution to journalArticle

Original languageEnglish
JournalEuropean Journal of Neurology
Volume19
Issue number11
DOIs
Publication statusPublished - Nov 2012

Keywords

  • FA2H
  • fatty acid hydroxylase-associated neurodegeneration
  • Leukodystrophy
  • Mutation
  • Spastic paraparesis
  • SPG35

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

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