N19S, a new SOD1 mutation in sporadic amyotrophic lateral sclerosis: no evidence for disease causation

Ann Neurol. 2003 Jun;53(6):815-8. doi: 10.1002/ana.10605.

Abstract

In a group of 331 sporadic amyotrophic lateral sclerosis (ALS) cases, we identified a new Cu/Zn superoxide dismutase single base substitution, N19S, in two patients. In the first case, seven healthy family members of 15 carried the substitution. Controls (n = 268) and familial ALS index cases (n = 180) were screened and one control subject with N19S was identified. Our data show that, despite a possible role of susceptibility factor for ALS, N19S alone cannot be considered as a direct cause for the disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age of Onset
  • Aged
  • Aged, 80 and over
  • Amyotrophic Lateral Sclerosis / epidemiology
  • Amyotrophic Lateral Sclerosis / genetics*
  • Female
  • Gene Expression
  • Genetic Carrier Screening / instrumentation
  • Humans
  • Male
  • Middle Aged
  • Pedigree
  • Point Mutation / genetics*
  • Superoxide Dismutase / genetics*
  • Superoxide Dismutase-1

Substances

  • SOD1 protein, human
  • Superoxide Dismutase
  • Superoxide Dismutase-1