Literature DB >> 18608106

Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy.

Francesca Luisa Conforti1, Teresa Sprovieri, Rosalucia Mazzei, Alessandra Patitucci, Carmine Ungaro, Stefano Zoccolella, Angela Magariello, Vincenzo La Bella, Alessandro Tessitore, Gioacchino Tedeschi, Isa Laura Simone, Giovanni Majorana, Paola Valentino, Luigi Citrigno, Annalia Gabriele, Francesco Bono, Maria Rosaria Monsurrò, Maria Muglia, Aldo Quattrone.   

Abstract

Mutations in the Cu/Zn superoxide dismutase 1 (SOD1) gene have been reported to cause adult-onset autosomal dominant amyotrophic lateral sclerosis (FALS). In sporadic cases (SALS), de novo mutations in the SOD1 gene have occasionally been observed. All the SOD1 mutations are autosomal dominantly inherited with the exception of D90A. To date, in Italy, only two sporadic ALS cases carrying the D90A mutation have been reported in a homozygous state. We investigated for the presence of this mutation in 169 unrelated ALS patients from southern Italy. The genetic analysis revealed three ALS patients (1.8%) with mild phenotype carrying the homozygous D90A mutation.

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Year:  2009        PMID: 18608106     DOI: 10.1080/17482960802163853

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler        ISSN: 1471-180X


  4 in total

1.  Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis.

Authors:  Marco Luigetti; Amelia Conte; Francesca Madia; Giuseppe Marangi; Marcella Zollino; Irene Mancuso; Michele Dileone; Alessandra Del Grande; Vincenzo Di Lazzaro; Pietro Attilio Tonali; Mario Sabatelli
Journal:  Neurol Sci       Date:  2009-08-15       Impact factor: 3.307

Review 2.  A Systematic Review of Genotype-Phenotype Correlation across Cohorts Having Causal Mutations of Different Genes in ALS.

Authors:  Owen Connolly; Laura Le Gall; Gavin McCluskey; Colette G Donaghy; William J Duddy; Stephanie Duguez
Journal:  J Pers Med       Date:  2020-06-29

3.  Cellular analysis of SOD1 protein-aggregation propensity and toxicity: a case of ALS with slow progression harboring homozygous SOD1-D92G mutation.

Authors:  Masanori Sawamura; Keiko Imamura; Rie Hikawa; Takako Enami; Ayako Nagahashi; Hodaka Yamakado; Hidenori Ichijo; Takao Fujisawa; Hirofumi Yamashita; Sumio Minamiyama; Misako Kaido; Hiromi Wada; Makoto Urushitani; Haruhisa Inoue; Naohiro Egawa; Ryosuke Takahashi
Journal:  Sci Rep       Date:  2022-07-25       Impact factor: 4.996

4.  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

  4 in total

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