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dc.contributor.author
Schollen, E.
dc.contributor.author
Frank, C.G.
dc.contributor.author
Keldermans, L.
dc.contributor.author
Reyntjens, R.
dc.contributor.author
Grubenmann, C.E.
dc.contributor.author
Clayton, P.T.
dc.contributor.author
Winchester, B.G.
dc.contributor.author
Smeitink, J.
dc.contributor.author
Wevers, R.A.
dc.contributor.author
Aebi, M.
dc.contributor.author
Hennet, T.
dc.contributor.author
Matthijs, G.
dc.date.accessioned
2017-06-10T01:25:36Z
dc.date.available
2017-06-10T01:25:36Z
dc.date.issued
2004-07
dc.identifier.issn
0022-2593
dc.identifier.issn
1468-6244
dc.identifier.other
10.1136/jmg.2003.016923
dc.identifier.uri
http://hdl.handle.net/20.500.11850/50042
dc.language.iso
en
dc.publisher
BMJ
dc.title
Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency)
dc.type
Journal Article
ethz.journal.title
Journal of medical genetics
ethz.journal.volume
41
ethz.journal.issue
7
ethz.journal.abbreviated
J Med Genet
ethz.pages.start
550
ethz.pages.end
556
ethz.notes
Received 4 December 2003, Accepted 6 February 2004.
ethz.identifier.wos
ethz.publication.place
London
ethz.publication.status
published
ethz.date.deposited
2017-06-10T01:26:13Z
ethz.source
ECIT
ethz.identifier.importid
imp59364f4a7225c47137
ethz.ecitpid
pub:82027
ethz.eth
yes
ethz.availability
Metadata only
ethz.rosetta.installDate
2017-07-12T22:07:03Z
ethz.rosetta.lastUpdated
2024-02-01T18:46:48Z
ethz.rosetta.versionExported
true
ethz.COinS
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