Orphanet: Biochemical diagnosis of Peroxisomal disorders Analyte: Very Long Chain Fatty Acids VLCFA
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Biochemical diagnosis of Peroxisomal disorders (Analyte: Very Long Chain Fatty Acids - VLCFA)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 07/03/2011
  • Biochemical Genetics Unit
  • Box 247, Department of Clinical Biochemistry and Immunology
  • Addenbrooke's Hospital
  • Hills Road
  • CAMBRIDGE CB2 0QQ
  • UNITED KINGDOM
  • Director of laboratory : Dr Jacqui CALVIN
  • More information
  • Phone : 44 (0)1223 245151
  • Additional Phone : -
  • Fax : 44 (0)1223 216 867
  • Website
Last update: March 2011

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Biochemical genetics
Analyte / Enzyme assay
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