A SPG3A mutation with a novel foot phenotype of hereditary spastic paraplegia in a Chinese Han family

Chin Med J (Engl). 2007 May 5;120(9):834-7.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Child
  • Child, Preschool
  • China / ethnology
  • Evoked Potentials, Somatosensory
  • Evolution, Molecular
  • Female
  • Foot Deformities, Congenital / genetics*
  • GTP Phosphohydrolases / genetics*
  • GTP-Binding Proteins
  • Genes, Dominant*
  • Humans
  • Male
  • Membrane Proteins
  • Middle Aged
  • Mutation*
  • Spastic Paraplegia, Hereditary / genetics*

Substances

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