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 journalArticle

Original languageEnglish
JournalEuropean Journal of Neurology
Volume21
Issue number3
DOIs
Publication statusPublished - Mar 2014

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

Cite this