A DEFICIENCY IN COG1 CAUSES A NOVEL CONGENITAL DISORDER OF GLYCOSYLATION TYPE II

Research output: Contribution to journalSpecial issue

Author(s)

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

Department/unit(s)

Publication details

JournalJournal of inherited metabolic disease
DatePublished - 2005
Volume28
Number of pages1
Pages (from-to)202-202
Original languageEnglish

Discover related content

Find related publications, people, projects, datasets and more using interactive charts.

View graph of relations