Orphanet: Biochemical diagnosis of Peroxisomal disorders Analyte: Pristanic acid
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Biochemical diagnosis of Peroxisomal disorders (Analyte: Pristanic acid)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 17/07/2014
  • Paediatric Metabolic Section, Department of Clinical Biochemistry
  • Newcastle upon Tyne Hospitals NHS Foundation Trust Royal
  • The Great North Children's Hospital, Royal Victoria Infirmary
  • Queen Victoria Road
  • NEWCASTLE UPON TYNE NE1 4LP
  • UNITED KINGDOM
  • Director of laboratory : Dr Kim BARTLETT
  • More information
  • Phone : 44 (0)191 282 4566
  • Additional Phone : -
  • Fax : 44 (0)191 282 4217
  • Website
Last update: July 2014

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Biochemical genetics
Analyte / Enzyme assay
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