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Browsing by Author Cantagrel, V.
Showing results 1 to 4 of 4
| Full Text | Issue Date | Title | Author(s) | | 2011 | Normal glycosylation screening does not rule out SRD5A3-CDG | Mohamed, M.; Cantagrel, V.; Al-Gazali, L.; Wevers, R.A.; Lefeber, D.J., et al |
| 2011 | From glycosylation disorders to dolichol biosynthesis defects: a new class of metabolic diseases | Cantagrel, V.; Lefeber, D.J. |
| 2010 | A novel cerebello-ocular syndrome with abnormal glycosylation due to abnormalities in dolichol metabolism. | Morava, E.; Wevers, R.A.; Cantagrel, V.; Hoefsloot, L.H.; Al-Gazali, L., et al |
| 2010 | SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder. | Cantagrel, V.; Lefeber, D.J.; Ng, B.G.; Guan, Z.; Silhavy, J.L., et al |
Showing results 1 to 4 of 4
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