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Neuromuscular dysfunction in the mutant superoxide dismutase mouse model of amyotrophic lateral sclerosis

✍ Scribed by Parkhouse, Wade S.; Cunningham, Lori; McFee, Ingrid; Litt Miller, Jennifer M.; Whitney, Darryl; Pelech, Steven L.; Krieger, Charles

Book ID
120389661
Publisher
Informa plc
Year
2008
Tongue
English
Weight
733 KB
Volume
9
Category
Article
ISSN
1471-180X

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## Abstract High molecular weight detergent‐insoluble complexes of superoxide dismutase 1 (SOD1) enzyme are a biochemical abnormality associated with mutant SOD1‐linked familial amyotrophic lateral sclerosis (FALS). In the present study, SOD1 protein from spinal cords of transgenic FALS mice was fr