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Phenotype in an Infant with SOD1 Homozygous Truncating Mutation
Umeå University, Faculty of Medicine, Department of Pharmacology and Clinical Neuroscience, Clinical Neuroscience.
Umeå University, Faculty of Medicine, Department of Pharmacology and Clinical Neuroscience, Clinical Neuroscience.
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2019 (English)In: New England Journal of Medicine, ISSN 0028-4793, E-ISSN 1533-4406, Vol. 381, no 5, p. 486-488Article in journal, Letter (Refereed) Published
Place, publisher, year, edition, pages
Massachusetts Medical Society , 2019. Vol. 381, no 5, p. 486-488
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Neurosciences
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URN: urn:nbn:se:umu:diva-162395DOI: 10.1056/NEJMc1905039ISI: 000478064200016PubMedID: 31314961OAI: oai:DiVA.org:umu-162395DiVA, id: diva2:1344219
Available from: 2019-08-20 Created: 2019-08-20 Last updated: 2019-08-20Bibliographically approved

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Andersen, Peter M.Nordström, UlrikaZetterström, PerMarklund, Stefan L.

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Clinical NeuroscienceDepartment of Medical Biosciences
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