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Biochemical diagnosis of Congenital Disorder of Glycosylation, type Ia (Analyte: Phosphomannomutase)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 11/11/2009
  • Laboratorium Enzymdiagnostiek
  • Afdeling Klinische Genetica - Sectie Genetische Metabole Ziekten
  • Erasmus MC, Faculteitsgebouw
  • Dr. Molewaterplein 50
  • Director of laboratory : Dr F.W. [Frans] VERHEIJEN
  • More information
  • Phone : 31 (0)10 7043212
  • Additional Phone : -
  • Fax : 31 (0)10 7043200
  • Website
  • Contact
Last update: November 2009

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Biochemical genetics
Analyte / Enzyme assay

List of diseases and genes

List of diseases tested (1)
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