Treatment of hereditary tyrosinaemia (fumarylacetoacetase deficiency) by enzyme substitution
- 1 June 1986
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 9 (S2) , 257-261
- https://doi.org/10.1007/bf01799722
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- POSSIBILITIES FOR TREATMENT AND FOR EARLY PRENATAL DIAGNOSIS OF HEREDITARY TYROSINAEMIAThe Lancet, 1985
- Deficient Fumarylacetoacetate Fumarylhydrolase Activity in Lymphocytes and Fibroblasts from Patients with Hereditary TyrosinemiaPediatric Research, 1983
- Hereditary tyrosinemia - fumarylacetoacetase deficiencyPediatric Research, 1979
- On the enzymic defects in hereditary tyrosinemia.Proceedings of the National Academy of Sciences, 1977
- The occurrence of hepatoma in the chronic form of hereditary tyrosinemiaThe Journal of Pediatrics, 1976