DETECTION OF PHENYLALANINE HYDROXYLASE MESSENGER RNA IN LIVER BIOPSY SAMPLES FROM PATIENTS WITH PHENYLKETONURIA
- 19 January 1985
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 325 (8421) , 160-161
- https://doi.org/10.1016/s0140-6736(85)91925-7
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuriaNature, 1983
- Polysome immunoprecipitation of phenylalanine hydroxylase mRNA from rat liver and cloning of its cDNA.Proceedings of the National Academy of Sciences, 1982
- Studies on the molecular defect in phenylketonuria and hyperphenylalaninaemia using antibodies against phenylalanine hydroxylaseJournal of Inherited Metabolic Disease, 1982
- Observations indicating the nature of the mutation in phenylketonuriaJournal of Inherited Metabolic Disease, 1979
- Detection of Hepatic Phenylalanine 4-Hydroxylase in Classical PhenylketonuriaProceedings of the National Academy of Sciences, 1973
- Nature of the Molecular Defect in Phenylketonuria and HyperphenylalaninaemiaNature, 1972