Literature DB >> 8682505

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

M Kostrzewa1, M S Damian, U Müller.   

Abstract

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.

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Year:  1996        PMID: 8682505     DOI: 10.1007/s004390050157

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  4 in total

1.  The epidemiology of CuZn-SOD mutations in Germany: a study of 217 families.

Authors:  Malessa Rabe; Ansgar Felbecker; Stefan Waibel; Peter Steinbach; Pia Winter; Ulrich Müller; Albert C Ludolph
Journal:  J Neurol       Date:  2010-03-23       Impact factor: 4.849

Review 2.  Immature copper-zinc superoxide dismutase and familial amyotrophic lateral sclerosis.

Authors:  Sai V Seetharaman; Mercedes Prudencio; Celeste Karch; Stephen P Holloway; David R Borchelt; P John Hart
Journal:  Exp Biol Med (Maywood)       Date:  2009-07-13

3.  Oxidative stress and superoxide dismutase in development, aging and gene regulation.

Authors:  R G Allen
Journal:  Age (Omaha)       Date:  1998-04

4.  Protein aggregation and protein instability govern familial amyotrophic lateral sclerosis patient survival.

Authors:  Qi Wang; Joshua L Johnson; Nathalie Y R Agar; Jeffrey N Agar
Journal:  PLoS Biol       Date:  2008-07-29       Impact factor: 8.029

  4 in total

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