The autosomal recessive form of CMT disease linked to 5q31-q33

Ann N Y Acad Sci. 1999 Sep 14:883:56-9.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Algeria
  • Charcot-Marie-Tooth Disease / genetics*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 5*
  • Consanguinity
  • Female
  • Genes, Recessive
  • Genetic Linkage
  • Genetic Markers
  • Humans
  • Male

Substances

  • Genetic Markers