Literature DB >> 11284995

Sporadic ALS associated with the D90A Cu,Zn superoxide dismutase mutation in Russia.

V I Skvortsova1, S A Limborska, P A Slominsky, N I Levitskaya, G N Levitsky, M I Shadrina, E A Kondratyeva.   

Abstract

Twenty blood samples from Russian patients (Moscow) with idiopathic motor neurone disease were analysed for mutations in the Cu,Zn superoxide dismutase (Cu,Zn SOD) gene. Two patients (10%) with the amyotrophic lateral sclerosis (ALS) form of the disease were found to have a disease-related mutation. One patient appears to have autosomal recessive adult-onset ALS associated with homozygosity for D90A and presents the characteristic phenotype of very slowly ascending paresis with both lower and upper motor neurone signs. Another patient, heterozygous for D90A, presents ALS with lumbar onset and rapid progression. This is the first report of a Cu,Zn SOD mutation in ALS in Russia.

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Year:  2001        PMID: 11284995     DOI: 10.1046/j.1468-1331.2001.00186.x

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  2 in total

1.  FUS gene mutations associated with familiar forms of amyotrophic lateral sclerosis affect cellular localization and aggregation properties of the encoded protein.

Authors:  T A Shelkovnikova; A A Ustyugov; A P Smirnov; V I Skvortsova; V L Buchman; S O Bachurin; N N Ninkina
Journal:  Dokl Biochem Biophys       Date:  2011-07-03       Impact factor: 0.788

2.  Individual Oligogenic Background in p.D91A-SOD1 Amyotrophic Lateral Sclerosis Patients.

Authors:  Giulia Gentile; Benedetta Perrone; Giovanna Morello; Isabella Laura Simone; Sebastiano Andò; Sebastiano Cavallaro; Francesca Luisa Conforti
Journal:  Genes (Basel)       Date:  2021-11-23       Impact factor: 4.096

  2 in total

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