Neonatal screening for dihydropteridine reductase deficiency
- 1 June 1985
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 8 (S2) , 99-100
- https://doi.org/10.1007/bf01811477
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Tetrahydrobiopterin deficiencies: Preliminary analysis from an international surveyThe Journal of Pediatrics, 1984
- Blood spots on Guthrie cards can be used for inherited tetrahydrobiopterin deficiency screening in hyperphenylalaninaemic infants.Archives of Disease in Childhood, 1984
- Hyperphenylalaninemia Due to Dihydropteridine Reductase Deficiency: Diagnosis by Enzyme Assays on Dried Blood SpotsPediatrics, 1982
- Malignant hyperphenylalaninaemia—Current status (June 1977)Journal of Inherited Metabolic Disease, 1978