Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Chinese Han patients with hereditary spastic paraplegia

Chin Med J (Engl). 2009 Sep 5;122(17):2064-6.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Asian People / genetics*
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Infant
  • Male
  • Membrane Transport Proteins / genetics*
  • Middle Aged
  • Mutation / genetics*
  • Polymerase Chain Reaction
  • Sequence Analysis, DNA
  • Spastic Paraplegia, Hereditary / genetics*
  • Young Adult

Substances

  • Membrane Transport Proteins
  • REEP1 protein, human