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 journalLetter

9 Scopus citations
Original languageEnglish (US)
Pages (from-to)e25-e26
JournalEuropean Journal of Neurology
Volume21
Issue number3
DOIs
StatePublished - Mar 1 2014

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

Cite this

Magariello, A., Citrigno, L., Zuchner, S., Gonzalez, M., Patitucci, A., Sofia, V., Conforti, F. L., Pappalardo, I., Mazzei, R., Ungaro, C., Zappia, M., & Muglia, M. (2014). Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum. European Journal of Neurology, 21(3), e25-e26. https://doi.org/10.1111/ene.12305