Direkt zum Inhalt
Merck
  • Superoxide dismutase 1: identification of a novel mutation in a case of familial amyotrophic lateral sclerosis.

Superoxide dismutase 1: identification of a novel mutation in a case of familial amyotrophic lateral sclerosis.

Human genetics (1996-07-01)
M Kostrzewa, M S Damian, U Müller
ZUSAMMENFASSUNG

Mutation analysis of the superoxide dismutase gene SOD1 in a familial case of amyotrophic lateral sclerosis revealed a T --> C transition at codon 151 of exon 5. This mutation results in the substitution of an isoleucine for a threonine. It appears to affect formation of dimers of the protein and is the most C-terminal amino acid change in SOD1 described to date.