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Phenotype in an Infant with
SOD1
Homozygous Truncating Mutation
Andersen, Peter M.
Umeå University, Faculty of Medicine, Department of Pharmacology and Clinical Neuroscience, Clinical Neuroscience.
ORCID iD:
0000-0003-0094-5429
Hempel, Maja
Santer, René
Nordström, Ulrika
Umeå University, Faculty of Medicine, Department of Pharmacology and Clinical Neuroscience, Clinical Neuroscience.
Tsiakas, Konstantinos
Johannsen, Jessika
Volk, Alexander E.
Bierhals, Tatjana
Zetterström, Per
Umeå University, Faculty of Medicine, Department of Medical Biosciences, Clinical chemistry.
Marklund, Stefan L.
Umeå University, Faculty of Medicine, Department of Medical Biosciences, Clinical chemistry.
ORCID iD:
0000-0002-3270-2854
Show others and affiliations
2019 (English)
In:
New England Journal of Medicine, ISSN 0028-4793, E-ISSN 1533-4406, Vol. 381, no 5, p. 486-488
Article in journal, Letter (Refereed) Published
Place, publisher, year, edition, pages
Massachusetts Medical Society , 2019. Vol. 381, no 5, p. 486-488
National Category
Neurosciences
Identifiers
URN:
urn:nbn:se:umu:diva-162395
DOI:
10.1056/NEJMc1905039
ISI:
000478064200016
PubMedID:
31314961
Scopus ID:
2-s2.0-85070850141
OAI: oai:DiVA.org:umu-162395
DiVA, id:
diva2:1344219
Available from:
2019-08-20
Created:
2019-08-20
Last updated:
2024-07-02
Bibliographically approved
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Andersen, Peter M.
Nordström, Ulrika
Zetterström, Per
Marklund, Stefan L.
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