Identification and functional analysis of a defect in the human ALG9 gene
Definition of congenital disorder of glycosylation type IL
dc.contributor.author
Frank, Christian G.
dc.contributor.author
Eyaid, Wafaa
dc.contributor.author
Berger, Eric G.
dc.contributor.author
Aebi, Markus
dc.contributor.author
Grubenmann, Claudia E.
dc.contributor.author
Hennet, Thierry
dc.date.accessioned
2017-06-10T01:32:32Z
dc.date.available
2017-06-10T01:32:32Z
dc.date.issued
2004-07
dc.identifier.issn
0002-9297
dc.identifier.issn
1537-6605
dc.identifier.other
10.1086/422367
dc.identifier.uri
http://hdl.handle.net/20.500.11850/50182
dc.language.iso
en
dc.publisher
Cell Press
dc.title
Identification and functional analysis of a defect in the human ALG9 gene
dc.type
Journal Article
ethz.title.subtitle
Definition of congenital disorder of glycosylation type IL
ethz.journal.title
American Journal of Human Genetics
ethz.journal.volume
75
ethz.journal.issue
1
ethz.journal.abbreviated
Am J Hum Genet
ethz.pages.start
146
ethz.pages.end
150
ethz.notes
Received 2 March 2004, Accepted 4 May 2004, Published online 21 December 2007.
ethz.identifier.wos
ethz.identifier.nebis
000981285
ethz.publication.place
New York, NY
ethz.publication.status
published
ethz.date.deposited
2017-06-10T01:34:20Z
ethz.source
ECIT
ethz.identifier.importid
imp59364f4d574f214264
ethz.ecitpid
pub:82168
ethz.eth
yes
ethz.availability
Metadata only
ethz.rosetta.installDate
2017-07-12T20:05:01Z
ethz.rosetta.lastUpdated
2024-02-01T18:47:26Z
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