Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia

Ann Neurol. 2002 Jun;51(6):794-5. doi: 10.1002/ana.10185.
No abstract available

Publication types

  • Letter

MeSH terms

  • Child
  • Chromosomes, Human, Pair 14 / genetics
  • GTP Phosphohydrolases / genetics*
  • GTP-Binding Proteins
  • Genes, Dominant / genetics
  • Humans
  • Italy
  • Membrane Proteins
  • Point Mutation*
  • Sequence Analysis, DNA
  • Spastic Paraplegia, Hereditary / genetics*

Substances

  • Membrane Proteins
  • ATL1 protein, human
  • GTP Phosphohydrolases
  • GTP-Binding Proteins