| Literature DB >> 12402272 |
Michael D Alexander1, Bryan J Traynor, Nicole Miller, Bernie Corr, Eithne Frost, Shirley McQuaid, Francesca M Brett, Andrew Green, Orla Hardiman.
Abstract
Mutations in the Cu/Zn superoxide dismutase gene (SOD-1) are reported in 20% of familial amyotrophic lateral sclerosis (ALS) cases, but no definite report of a mutation in a "truly" sporadic case of ALS has been proved. We present the first case of a novel SOD-1 mutation in a patient with genetically proven sporadic ALS. This mutation (H80A) is believed to alter zinc ligand binding, and its functional significance correlates well with the aggressive clinical course and postmortem findings observed in this patient.Entities:
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Year: 2002 PMID: 12402272 DOI: 10.1002/ana.10369
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422