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Researcher
Wendy Vleugels
- Disciplines:Diagnostics, Laboratory medicine, Medicinal products
Affiliations
- Laboratory for Molecular Diagnosis (Division)
Member
From1 Apr 2009 → 30 Nov 2009 - Department of Human Genetics (Department)
Member
From15 Nov 2004 → 31 Mar 2009
Publications
1 - 5 of 5
- RFT1-CDG: Deafness as a novel feature of congenital disorders of glycosylation(2009)
Authors: Wendy Vleugels, Luc Régal, Nathalie Goemans, François Foulquier, Gert Matthijs
Pages: 335 - 338 - RFT1 deficiency in three novel CDG patients(2009)
Authors: Wendy Vleugels, François Foulquier, Gert Matthijs
Pages: 1428 - 1434 - Quality control of glycoproteins bearing truncated glycans in an ALG9 defective (CDG-IL) patient(2009)
Authors: Wendy Vleugels, Gert Matthijs, François Foulquier
Pages: 910 - 917 - Screening for OST deficiencies in unsolved CDG-I patients(2009)
Authors: Wendy Vleugels, François Foulquier, Gert Matthijs
Pages: 769 - 774 - Mammalian phosphomannomutase PMM1 is the brain IMP-sensitive glucose-1,6-bisphosphatase(2008)
Authors: Wendy Vleugels, Gert Matthijs
Pages: 33988 - 33993