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

Eur J Neurol. 2014 Mar;21(3):e25-6. doi: 10.1111/ene.12305.
No abstract available

Publication types

  • Letter

MeSH terms

  • Corpus Callosum / pathology*
  • Family Health
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Mutation / genetics*
  • Phospholipases / genetics*
  • Spastic Paraplegia, Hereditary / genetics*
  • Spastic Paraplegia, Hereditary / pathology*

Substances

  • Phospholipases
  • DDHD2 protein, human