Familial amyotrophic lateral sclerosis/motor neurone disease (FALS): a review of current developments

J Med Genet. 1995 Nov;32(11):841-7. doi: 10.1136/jmg.32.11.841.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Age of Onset
  • Aged
  • Aged, 80 and over
  • Amyotrophic Lateral Sclerosis / classification
  • Amyotrophic Lateral Sclerosis / epidemiology
  • Amyotrophic Lateral Sclerosis / genetics*
  • Animals
  • Chromosomes, Human, Pair 21 / genetics
  • Ciliary Neurotrophic Factor
  • Disease Models, Animal
  • Female
  • Genes, Dominant
  • Genetic Linkage
  • Genetic Testing
  • Humans
  • Infant
  • Intermediate Filaments / pathology
  • Male
  • Mice
  • Middle Aged
  • Motor Neurons / pathology
  • Nerve Tissue Proteins / deficiency
  • Nerve Tissue Proteins / genetics
  • Neurofilament Proteins / analysis
  • Pedigree
  • Point Mutation
  • Superoxide Dismutase / chemistry
  • Superoxide Dismutase / deficiency*
  • Superoxide Dismutase / genetics

Substances

  • Ciliary Neurotrophic Factor
  • Nerve Tissue Proteins
  • Neurofilament Proteins
  • Superoxide Dismutase