Phenotypic manifestations in French-Canadian populations with Charcot-Marie-Tooth disease type 1A associated with 17p11.2 duplication

Ann N Y Acad Sci. 1999 Sep 14:883:497-9.
No abstract available

MeSH terms

  • Adult
  • Charcot-Marie-Tooth Disease / genetics*
  • Charcot-Marie-Tooth Disease / physiopathology
  • Child
  • Chromosome Mapping
  • Chromosomes, Human, Pair 17*
  • France / ethnology
  • Gene Duplication*
  • Humans
  • Phenotype
  • Quebec