The Antenatal Diagnosis and Aid to the Management of Hereditary Tyrosinaemia by Use of a Specific and Sensitive GC—MS Assay for Succinylacetone
- 1 January 1984
- book chapter
- Published by Springer Nature
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Detection of succinylacetone and the use of its measurement in mass screening for hereditary tyrosinemiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1982
- Prenatal diagnosis of hereditary tyrosinaemia: Measurement of succinylacetone in amniotic fluidPrenatal Diagnosis, 1982
- Urinary excretion of succinylacetone and δ-aminolevulinic acid in patients with hereditary tyrosinemiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1981
- Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1981
- On the enzymic defects in hereditary tyrosinemia.Proceedings of the National Academy of Sciences, 1977