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Rare coding variants in the mme gene, encoding the metalloprotease neprilysin, are linked to late-onset axonal neuropathies
Umeå University, Faculty of Medicine, Department of Pharmacology and Clinical Neuroscience, Clinical Neuroscience.
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2016 (English)In: Journal of the peripheral nervous system, ISSN 1085-9489, E-ISSN 1529-8027, Vol. 21, no 3, p. 235-235Article in journal, Meeting abstract (Other academic) Published
Place, publisher, year, edition, pages
Wiley-Blackwell, 2016. Vol. 21, no 3, p. 235-235
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Neurosciences
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URN: urn:nbn:se:umu:diva-126747DOI: 10.1111/jns.12181ISI: 000383856200217OAI: oai:DiVA.org:umu-126747DiVA, id: diva2:1038625
Conference
6th International Charcot-Marie-Tooth and Related Neuropathy Consortium (CMTR) Meeting, Venice - Mestre (Italy), 8-10 September, 2016.
Available from: 2016-10-19 Created: 2016-10-13 Last updated: 2018-06-09Bibliographically approved

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Andersen, Peter

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