Dominant GDAP1 mutations cause predominantly mild CMT phenotypes
dc.contributor.author
Zimoń, M.
dc.contributor.author
Huber, N.
dc.contributor.author
Niemann, Axel
dc.contributor.author
et al.
dc.date.accessioned
2017-11-24T14:14:26Z
dc.date.available
2017-06-09T13:12:42Z
dc.date.available
2017-11-24T14:14:26Z
dc.date.issued
2011-08
dc.identifier.issn
0028-3878
dc.identifier.other
10.1212/WNL.0b013e318228fc70
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/38524
dc.language.iso
en
en_US
dc.publisher
Lippincott Williams & Wilkins
dc.title
Dominant GDAP1 mutations cause predominantly mild CMT phenotypes
en_US
dc.type
Journal Article
ethz.journal.title
Neurology
ethz.journal.volume
77
en_US
ethz.journal.issue
6
en_US
ethz.pages.start
540
en_US
ethz.pages.end
548
en_US
ethz.identifier.wos
ethz.identifier.nebis
004669172
ethz.publication.place
Hagerstown, MD
ethz.publication.status
published
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02030 - Dep. Biologie / Dep. of Biology::02539 - Institut für Molecular Health Sciences / Institute of Molecular Health Sciences::03367 - Suter, Ulrich / Suter, Ulrich
en_US
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02030 - Dep. Biologie / Dep. of Biology::02539 - Institut für Molecular Health Sciences / Institute of Molecular Health Sciences::03367 - Suter, Ulrich / Suter, Ulrich
ethz.date.deposited
2017-06-09T13:13:05Z
ethz.source
ECIT
ethz.identifier.importid
imp59364e4fb531b79511
ethz.ecitpid
pub:62176
ethz.eth
yes
en_US
ethz.availability
Metadata only
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ethz.rosetta.installDate
2017-07-15T09:37:18Z
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2024-02-02T03:16:02Z
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true
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Journal Article [128813]