High frequency of mutations in codon 98 of the peripheral myelin protein P0 gene in 20 French CMT1 patients

Am J Hum Genet. 1996 Mar;58(3):638-41.
No abstract available

Publication types

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

MeSH terms

  • Base Sequence
  • Charcot-Marie-Tooth Disease / genetics*
  • Charcot-Marie-Tooth Disease / physiopathology
  • Codon / genetics*
  • DNA Mutational Analysis*
  • Female
  • Humans
  • Male
  • Molecular Sequence Data
  • Myelin P0 Protein / genetics*
  • Pedigree

Substances

  • Codon
  • Myelin P0 Protein