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Progressive aphasia as the presenting symptom in a patient with amyotrophic lateral sclerosis with a novel mutation in the OPTN gene
Kantonsspital, Neuromuscular Dis Unit, ALS Clin, CH-9007 St Gallen, Switzerland.
Umeå University, Faculty of Medicine, Department of Pharmacology and Clinical Neuroscience, Clinical Neuroscience.
Kantonsspital, Neuromuscular Dis Unit, ALS Clin, CH-9007 St Gallen, Switzerland.
Jichi Med Univ, Dept Neurol, Shimotsuke, Japan.
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2013 (English)In: Amyotrophic Lateral Sclerosis and Frontootemporal Degeneration, ISSN 2167-8421, Vol. 14, no 2, p. 138-140Article in journal (Refereed) Published
Place, publisher, year, edition, pages
Informa Healthcare, 2013. Vol. 14, no 2, p. 138-140
Keyword [en]
Amyotrophic lateral sclerosis, optineurin, mutation, phenotype
National Category
Neurosciences
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URN: urn:nbn:se:umu:diva-67790DOI: 10.3109/21678421.2012.756525ISI: 000315416500010OAI: oai:DiVA.org:umu-67790DiVA, id: diva2:614151
Available from: 2013-04-03 Created: 2013-04-03 Last updated: 2018-06-08Bibliographically approved

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Andersen, Peter M

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