Deficiency of the first mannosylation step in the N glycosylation pathway causes congenital disorder of glycosylation type Ik
- Journal Article
Rights / licenseIn Copyright - Non-Commercial Use Permitted
Journal / seriesHuman Molecular Genetics
Pages / Article No.
PublisherOxford University Press
NotesReceived 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 publisher
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