SOD1 missense mutation in an Italian family with ALS

Neurology. 1994 Feb;44(2):347-9. doi: 10.1212/wnl.44.2.347.

Abstract

We have discovered a new Italian pedigree with autosomal-dominant ALS. The pedigree, at present, comprises 75 members distributed in five generations. ALS was diagnosed in eight patients. The mean +/- SD age of onset of the disease was 46.8 +/- 13.5 years, with a range of 29 to 63 years. The mean +/- SD duration of the disease was 11.6 +/- 1.7 months. Molecular genetic studies showed a missense mutation (Gly-->Ser, codon 41) in exon 2 of the Cu/Zn superoxide dismutase gene (SOD1) on chromosome 21 in the available affected member and in 45% of the at-risk subjects of the pedigree. This study confirms the presence of SOD1 point mutations in families with autosomal-dominant ALS and suggests that additional genetic or environmental factors may be involved in the full expression of the disease.

Publication types

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

MeSH terms

  • Adult
  • Amyotrophic Lateral Sclerosis / enzymology*
  • Amyotrophic Lateral Sclerosis / genetics*
  • Base Sequence
  • Chromosomes, Human, Pair 21*
  • DNA / blood
  • DNA Primers
  • Family
  • Female
  • Glycine
  • Humans
  • Italy
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Pedigree
  • Point Mutation*
  • Polymerase Chain Reaction
  • Serine
  • Superoxide Dismutase / genetics*

Substances

  • DNA Primers
  • Serine
  • DNA
  • Superoxide Dismutase
  • Glycine