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PMID: 12402272 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't

"True" sporadic ALS associated with a novel SOD-1 mutation.

Annals of neurology ·Vol. 52 ·No. 5 ·2002-11-00 ·Pages 680-3

Alexander MD, Traynor BJ, Miller N, Corr B, Frost E, McQuaid S, Brett FM, Green A, Hardiman O

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.

MeSH Terms
Adult Amyotrophic Lateral Sclerosis/genetics,pathology,physiopathology Humans Male Mutation/genetics Pedigree Superoxide Dismutase/genetics Superoxide Dismutase-1
Chemicals
SOD1 protein, human Superoxide Dismutase Superoxide Dismutase-1
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Alexander Michael D
Department of Neurology, Beaumont Hospital, Beaumont Road, Dublin 9, Ireland. [email protected]
Traynor Bryan J
Miller Nicole
Corr Bernie
Frost Eithne
McQuaid Shirley
Brett Francesca M
Green Andrew
Hardiman Orla
Article Info
Journal
Annals of neurology
Abbr.
Ann Neurol
ISSN
0364-5134
Published
2002-11-00
Pages
680-3
Language
English
Region
United States
NLM ID
7707449
Subset
IM
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