Molecular basis for nonphenylketonuria hyperphenylalaninemia
- 1 September 1992
- Vol. 14 (1), 1-5
- https://doi.org/10.1016/s0888-7543(05)80274-5
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reactionGenomics, 1989
- Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuriaThe Journal of Pediatrics, 1987
- Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell AnemiaScience, 1985
- Effects of oral phenylalanine load on plasma glucagon, insulin, amino acid and glucose concentrations in manScandinavian Journal of Clinical and Laboratory Investigation, 1978
- PHENYLALANINE HAS NO EFFECT ON DIHYDROPTERIDINE REDUCTASE ACTIVITY IN PHENYLKETONURIA FIBROBLASTSThe Lancet, 1977
- ON INDICATIONS FOR TREATMENT OF THE HYPERPHENYLALANINEMIC NEONATEActa Paediatrica, 1977
- Serum tyrosine within the first hour after an oral load of phenylalanineScandinavian Journal of Clinical and Laboratory Investigation, 1977
- PERSISTENT HYPERPHENYLALANINEMIAActa Paediatrica, 1972
- Transient hyperphenylalaninemiaThe Journal of Pediatrics, 1968
- ATYPICAL PHENYLKETONURIA IN SISTERS WITH NORMAL OFFSPRINGThe Lancet, 1961