Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum

A. Magariello, L. Citrigno, S. Zuchner, M. Gonzalez, A. Patitucci, V. Sofia, F. L. Conforti, I. Pappalardo, R. Mazzei, C. Ungaro, M. Zappia, M. Muglia

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
JournalEuropean Journal of Neurology
Issue number3
Publication statusPublished - Mar 2014

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

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