"Sporadic" motoneuron disease due to familial SOD1 mutation with low penetrance

Lancet. 1994 Dec;344(8939-8940):1773. doi: 10.1016/s0140-6736(94)92913-0.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Amyotrophic Lateral Sclerosis / genetics*
  • Humans
  • Male
  • Middle Aged
  • Pedigree
  • Point Mutation*
  • Superoxide Dismutase / genetics*

Substances

  • Superoxide Dismutase