Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy
dc.contributor.author
Kurth, Ingo
dc.contributor.author
Pamminger, Torsten
dc.contributor.author
Hennings, J. Christopher
dc.contributor.author
Soehendra, Désirée
dc.contributor.author
Huebner, Antje K.
dc.contributor.author
Rotthier, Annelies
dc.contributor.author
Baets, Jonathan
dc.contributor.author
Senderek, Jan
dc.contributor.author
Topaloglu, Haluk
dc.contributor.author
Farrell, Sandra A.
dc.contributor.author
Nürnberg, Gudrun
dc.contributor.author
Nürnberg, Peter
dc.contributor.author
Jonghe, Peter de
dc.contributor.author
Gal, Andreas
dc.contributor.author
Kaether, Christoph
dc.contributor.author
Timmerman, Vincent
dc.contributor.author
Hübner, Christian A.
dc.date.accessioned
2017-06-14T11:34:13Z
dc.date.available
2017-06-14T11:34:13Z
dc.date.issued
2009-11
dc.identifier.issn
1061-4036
dc.identifier.issn
1546-1718
dc.identifier.other
10.1038/ng.464
dc.identifier.uri
http://hdl.handle.net/20.500.11850/157011
dc.language.iso
en
dc.publisher
Nature
dc.title
Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy
dc.type
Journal Article
ethz.journal.title
Nature Genetics
ethz.journal.volume
41
ethz.journal.issue
11
ethz.journal.abbreviated
Nat Genet
ethz.pages.start
1179
ethz.pages.end
1181
ethz.notes
Published online 18 October 2009.
ethz.identifier.wos
ethz.identifier.nebis
001002213
ethz.publication.place
New York, NY
ethz.publication.status
published
ethz.date.deposited
2017-06-14T11:41:35Z
ethz.source
ECIT
ethz.identifier.importid
imp59364cdf3c95682572
ethz.ecitpid
pub:35281
ethz.eth
yes
ethz.availability
Metadata only
ethz.rosetta.installDate
2017-07-18T08:26:09Z
ethz.rosetta.lastUpdated
2024-02-02T01:28:59Z
ethz.rosetta.versionExported
true
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