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Biochemical diagnosis of hypoxanthine-guanine phosphoribosyltransferase deficiency
Despite our efforts to ensure that data is up to date, this activity has not been validated since 07/05/2012- U.O.C. Malattie Metaboliche Ereditarie
- Dipartimento della Salute della Donna e del Bambino
- Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano
- Via Orus 2B
- 35129 PADOVA
- ITALY
- Director of laboratory : Dr Alberto BURLINA
- More information
Last update: May 2012
Responsible of diagnostic test
Purpose(s)
Post-natal diagnosis
Technical procedure(s)
Biochemical genetics
Analyte / Enzyme assay
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List of diseases and genes
List of diseases tested
(1)
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