Orphanet: Biochemical diagnosis of Peroxisomal biogenesis disorders

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Biochemical diagnosis of Peroxisomal biogenesis disorders & Peroxisomal single enzyme defects (Analyte: Fatty acids very-long-chain)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 17/07/2014
  • Department of Clinical Chemistry
  • B Floor, Orange Wing, Pathology Block
  • The Sheffield Children's Hospital
  • Western Bank
  • Director of laboratory : Dr James BONHAM
  • More information
  • Phone : 44 (0)114 271 7307
  • Additional Phone : -
  • Fax : 44 (0)114 270 6121
  • Website
Last update: July 2014

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Biochemical genetics
Analyte / Enzyme assay
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