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Biochemical diagnosis of Congenital Disorders of Glycosylation (Analysis of Transferrin N-glycosylation and ApoCIII O-glycosylation by iso-electric focusing in plasma and CDG-II subtype identification by mass spectrometry of transferrin)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 05/11/2013
  • Translationeel Metabool Laboratorium
  • Afdeling Laboratoriumgeneeskunde
  • Radboudumc - Radboud universitair medisch centrum
  • Geert Grooteplein-Zuid 10
  • 6525 GA NIJMEGEN
  • NETHERLANDS
  • Director of laboratory : Pr L.P.W.J. [Bert] VAN DEN HEUVEL
  • More information
  • Phone : +31 (0)24 361 4567
  • Additional Phone : -
  • Fax : +31 (0)24 366 8754
  • Website
  • Contact
Last update: November 2013

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Biochemical genetics
Analyte / Enzyme assay
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Analyte / Enzyme assay
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List of diseases and genes

List of diseases tested (1)
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