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Article

G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype.

Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases - 1 Jan 2010

Battistini Stefania, Ricci Claudia, Giannini Fabio, Calzavara Silvia, Greco Giuseppe, Del Corona Alberto, Mancuso Michelangelo, Battistini Noè, Siciliano Gabriele, Carrera Paola

Abstract excerpt

More than 140 different mutations have been reported in the Cu/Zn superoxide dismutase-1 (SOD1) gene in patients with amyotrophic lateral sclerosis (ALS), some occurring as founder mutations. Occasionally, specific mutations are associated with a particular phenotype. We evaluated a possible geno...

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Identifiers

PMID: 19488901
DOI: 10.3109/17482960902995592

Genes

SOD1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19488901-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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