Search research publications and outputs

  1. 2005
  2. A DEFICIENCY IN COG1 CAUSES A NOVEL CONGENITAL DISORDER OF GLYCOSYLATION TYPE II

    Matthijs, G., Foulquier, F., Zeevaert, R., Jaeken, J., Quelhas, D., Vilarinho, L., Ungar, D., Krieger, M. & Annaert, W., 2005

    Special issue in Journal of inherited metabolic disease