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dc.contributor.authorMurphy, S. M.
dc.contributor.authorErnst, D.
dc.contributor.authorWei, Y.
dc.contributor.authorLaura, M.
dc.contributor.authorLiu, Y.-T.
dc.contributor.authorPolke, J.
dc.contributor.authorBlake, J.
dc.contributor.authorWiner, J.
dc.contributor.authorHoulden, H.
dc.contributor.authorHornemann, T.
dc.contributor.authorReilly, M. M.
dc.date.accessioned2013-05-29T10:10:10Z
dc.date.available2013-05-29T10:10:10Z
dc.date.issued2013-05-29
dc.identifier.citationHereditary sensory and autonomic neuropathy type 1 (HSANI) caused by a novel mutation in SPTLC2 2013 Neurologyen_GB
dc.identifier.issn0028-3878
dc.identifier.issn1526-632X
dc.identifier.doi10.1212/WNL.0b013e318295d789
dc.identifier.urihttp://hdl.handle.net/10147/293002
dc.language.isoenen
dc.relation.urlhttp://www.neurology.org/cgi/doi/10.1212/WNL.0b013e318295d789en_GB
dc.rightsArchived with thanks to Neurologyen_GB
dc.titleHereditary sensory and autonomic neuropathy type 1 (HSANI) caused by a novel mutation in SPTLC2en_GB
dc.typeArticleen
dc.identifier.journalNeurologyen_GB
dc.description.provinceLeinsteren


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