Deficiency of the first mannosylation step in the N glycosylation pathway causes congenital disorder of glycosylation type Ik
Open access
Date
2004-03-01Type
- Journal Article
ETH Bibliography
yes
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Permanent link
https://doi.org/10.3929/ethz-b-000051881Publication status
publishedExternal links
Journal / series
Human Molecular GeneticsVolume
Pages / Article No.
Publisher
Oxford University PressNotes
Received 29 October 2003, Revised 15 December 2003, Accepted 22 December 2003, Published online 6 January 2004. It was possible to publish this article open access thanks to a Swiss National Licence with the publisherMore
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ETH Bibliography
yes
Altmetrics