Paesold-Burda, P; Maag, C; Troxler, H; Foulquier, F; Kleinert, P; Schnabel, S; Baumgartner, M; Hennet, T (2009). Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation. Human Molecular Genetics, 18(22):4350-4356.
Hülsmeier, A J; Paesold-Burda, P; Hennet, T (2007). N-glycosylation site occupancy in serum glycoproteins using multiple reaction monitoring liquid chromatography-mass spectrometry. Molecular & Cellular Proteomics, 6(12):2132-2138.