Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11

J Med Genet. 2005 Mar;42(3):260-5. doi: 10.1136/jmg.2004.024364.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Algeria / ethnology
  • Charcot-Marie-Tooth Disease / ethnology
  • Charcot-Marie-Tooth Disease / genetics*
  • Charcot-Marie-Tooth Disease / pathology
  • Chromosome Mapping
  • Chromosomes, Human, Pair 12 / genetics*
  • Chromosomes, Human, Pair 13 / genetics*
  • Demyelinating Diseases / ethnology
  • Demyelinating Diseases / genetics*
  • Demyelinating Diseases / pathology
  • Female
  • Genes, Recessive
  • Genetic Testing
  • Homozygote*
  • Humans
  • Lebanon / ethnology
  • Male
  • Pedigree
  • Sural Nerve / pathology