GC-MS identification of urinary succinylacetone in two cases of hereditary tyrosinaemia
- 1 March 1982
- journal article
- Published by Springer Nature in Journal of Inherited Metabolic Disease
- Vol. 5 (S1) , 41-42
- https://doi.org/10.1007/bf01799819
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- 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
- Acute hereditary tyrosinaemia type I: Clinical, biochemical and haematological studies in twinsJournal of Inherited Metabolic Disease, 1980
- Hereditary tyrosinemia - fumarylacetoacetase deficiencyPediatric Research, 1979
- On the enzymic defects in hereditary tyrosinemia.Proceedings of the National Academy of Sciences, 1977