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A novel central motor conduction abnormality in D90A-homozygous patients with amyotrophic lateral sclerosis.
Umeå University, Faculty of Medicine, Pharmacology and Clinical Neuroscience, Neurology.
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2004 (English)In: Muscle Nerve, ISSN 0148-639X, Vol. 29, no 6, 790-4 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2004. Vol. 29, no 6, 790-4 p.
Keyword [en]
Adult, Aged, Amyotrophic Lateral Sclerosis/*genetics/*physiopathology, Electromyography, Female, Homozygote, Humans, Male, Middle Aged, Motor Neurons/*physiology, Muscle; Skeletal/innervation, Neural Conduction, Phenotype, Point Mutation, Reaction Time, Superoxide Dismutase/*genetics
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URN: urn:nbn:se:umu:diva-18106DOI: doi:10.1002/mus.20032PubMedID: 15170611OAI: oai:DiVA.org:umu-18106DiVA: diva2:157779
Available from: 2008-01-10 Created: 2008-01-10 Last updated: 2011-01-12Bibliographically approved

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