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- Andersen, Peter M.,1962-Umeå universitet,Klinisk neurovetenskap (author)
Phenotype in an Infant with SOD1 Homozygous Truncating Mutation
- Article/chapterEnglish2019
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- Massachusetts Medical Society,2019
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- LIBRIS-ID:oai:DiVA.org:umu-162395
- https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-162395URI
- https://doi.org/10.1056/NEJMc1905039DOI
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- Language:English
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- Hempel, Maja (author)
- Santer, René (author)
- Nordström, UlrikaUmeå universitet,Klinisk neurovetenskap(Swepub:umu)ulno0003 (author)
- Tsiakas, Konstantinos (author)
- Johannsen, Jessika (author)
- Volk, Alexander E. (author)
- Bierhals, Tatjana (author)
- Zetterström, PerUmeå universitet,Klinisk kemi(Swepub:umu)perzem02 (author)
- Marklund, Stefan L.Umeå universitet,Klinisk kemi(Swepub:umu)stma0003 (author)
- Umeå universitetKlinisk neurovetenskap (creator_code:org_t)
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- In:New England Journal of Medicine: Massachusetts Medical Society381:5, s. 486-4880028-47931533-4406
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