Genetic abnormalities in Friedreich's ataxia

N Engl J Med. 1997 Apr 3;336(14):1021; author reply 1022. doi: 10.1056/NEJM199704033361412.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Chromosomes, Human, Pair 9
  • Friedreich Ataxia / genetics*
  • Homozygote
  • Humans
  • Phenotype
  • Point Mutation
  • Trinucleotide Repeats*