Orphanet: Biochemical diagnosis of Hypophosphatasia Analyte: Phosphoethanolamine

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Biochemical diagnosis of Hypophosphatasia (Analyte: Phosphoethanolamine)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 23/07/2010
  • Biochemical Genetics Unit
  • Box 247, Department of Clinical Biochemistry and Immunology
  • Addenbrooke's Hospital
  • Hills Road
  • Director of laboratory : Dr Jacqui CALVIN
  • More information
  • Phone : 44 (0)1223 245151
  • Additional Phone : -
  • Fax : 44 (0)1223 216 867
  • Website
Last update: July 2010

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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