Abstract
We describe three sporadic ALS patients in which a D11Y SOD1 mutation was detected. All three patients disclosed a prolonged survival and a stereotypical distal limbs involvement in the initial stages of the disease. By this report we demonstrate that D11Y SOD1 mutation is associated with a peculiar phenotype and we confirm its probable pathogenetic role.
Copyright © 2011 Elsevier B.V. All rights reserved.
Publication types
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Case Reports
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Comparative Study
MeSH terms
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Aged
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Amino Acid Substitution / genetics
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Amyotrophic Lateral Sclerosis / diagnosis*
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Amyotrophic Lateral Sclerosis / genetics*
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Aspartic Acid / genetics
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Female
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Genetic Association Studies* / methods
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Humans
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Middle Aged
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Mutation / genetics*
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Superoxide Dismutase / genetics*
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Superoxide Dismutase-1
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Tyrosine / genetics
Substances
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SOD1 protein, human
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Aspartic Acid
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Tyrosine
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Superoxide Dismutase
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Superoxide Dismutase-1