Orphanet: Biochemical diagnosis of Short Chain 3 Hydroxy Acyl CoA Dehydrogenase Deficiency Short Chain 3 Hydroxy Acyl CoA Dehydrogenase activity
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Biochemical diagnosis of Short-Chain 3-Hydroxy-Acyl-CoA Dehydrogenase Deficiency (Short-Chain 3-Hydroxy-Acyl-CoA Dehydrogenase activity)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 26/03/2014
  • Laboratorium Genetische Metabole Ziekten - Enzymdiagnostiek
  • Afdeling Klinische Chemie
  • Amsterdam UMC, locatie AMC
  • Meibergdreef 9
  • 1105 AZ AMSTERDAM
  • NETHERLANDS
  • Director of laboratory : Pr R.J.A. [Ronald] WANDERS
  • More information
  • Phone : 31 (0)20 566 5393
  • Additional Phone : 31 (0)20 566 2026
  • Fax : 31 (0)20 696 2596
  • Website
  • Contact
Last update: March 2014

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Biochemical genetics
Analyte / Enzyme assay
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List of diseases and genes

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