N19S, a new SOD1 mutation in sporadic amyotrophic lateral sclerosis: No evidence for disease causation

In a group of 331 sporadic amyotrophic lateral sclerosis (ALS) cases, we identified a new Cu/Zn superoxide dismutase single base substitution, N19S, in two patients. In the first case, seven healthy family members of 15 carried the substitution. Controls (n = 268) and familial ALS index cases (n = 1...

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Veröffentlicht in:Annals of neurology 2003-06, Vol.53 (6), p.815-818
Hauptverfasser: Mayeux, Véronique, Corcia, Philippe, Besson, Gérard, Jafari-Schluep, Hélène-Farnase, Briolotti, Valérie, Camu, William
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Sprache:eng
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Zusammenfassung:In a group of 331 sporadic amyotrophic lateral sclerosis (ALS) cases, we identified a new Cu/Zn superoxide dismutase single base substitution, N19S, in two patients. In the first case, seven healthy family members of 15 carried the substitution. Controls (n = 268) and familial ALS index cases (n = 180) were screened and one control subject with N19S was identified. Our data show that, despite a possible role of susceptibility factor for ALS, N19S alone cannot be considered as a direct cause for the disease. Ann Neurol 2003;53:815–818
ISSN:0364-5134
1531-8249
DOI:10.1002/ana.10605