CYP7B1 mutations in French-Canadian hereditary spastic paraplegia subjects

Can J Neurol Sci. 2012 Jan;39(1):91-4. doi: 10.1017/s0317167100012774.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age of Onset
  • Canada / ethnology
  • Cytochrome P450 Family 7
  • DNA Mutational Analysis
  • Family Health*
  • Female
  • Gene Frequency
  • Genotype
  • Humans
  • Male
  • Mutation / genetics*
  • Spastic Paraplegia, Hereditary / genetics*
  • Steroid Hydroxylases / genetics*

Substances

  • Steroid Hydroxylases
  • Cytochrome P450 Family 7
  • CYP7B1 protein, human