Phenylketonuria in turkey: Experience with an enzymatic colorimetric test for measurement of serum phenylalanine
- 1 May 1990
- journal article
- Published by Springer Nature in Journal of Inherited Metabolic Disease
- Vol. 13 (3) , 295-297
- https://doi.org/10.1007/bf01799378
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- A convenient enzymatic method for the determination of 4-methyl-2-oxopentanoate in plasma: Comparison with high performance liquid chromatographie analysisClinica Chimica Acta; International Journal of Clinical Chemistry, 1989
- Monitoring of phenylketonuria: A colorimetric method for the determination of plasma phenylalanine using l-phenylalanine dehydrogenaseAnalytical Biochemistry, 1989
- DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish populationHuman Genetics, 1989
- Incidence of phenylketonuria and hyperphenylalaninaemia in a sample of the Turkish newborn populationJournal of Inherited Metabolic Disease, 1986