New forms of hereditary tyrosinemia type II in mink: Hepatic tyrosine aminotransferase defect
Open Access
- 14 February 2008
- journal article
- research article
- Published by Springer Nature in Hereditas
- Vol. 104 (2) , 215-222
- https://doi.org/10.1111/j.1601-5223.1986.tb00535.x
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- New Principles of Ion-Exchange Techniques Suitable to Sample Preparation and Group Separation of Natural Products Prior to Liquid ChromatographyJournal of Liquid Chromatography, 1984
- A new variant form of hypertyrosinaemia due to 4‐hydroxyphenylpyruvic acid oxidase deficiencyJournal of Inherited Metabolic Disease, 1982
- Tyrosine aminotransferase deficiency in mink (Mustela vision): A model for human tyrosinemia IIBiochemical Genetics, 1981
- Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1981
- Hereditary tyrosinemia - fumarylacetoacetase deficiencyPediatric Research, 1979
- Molecular Biology and Molecular Pathology of a Newly Described Molecular Disease – Tyrosinemia II (The Richner-Hanhart Syndrome)Pathobiology, 1978
- Assay, properties and tissue distribution of p-hydroxyphenylpyruvate hydroxylaseBiochimica et Biophysica Acta (BBA) - Enzymology, 1972
- Soluble and mitochondrial forms of tyrosine aminotransferase. Relation to human tyrosinemiaBiochemistry, 1969
- Dietary Treatment in Tyrosinemia (Tyrosinosis)American Journal of Diseases of Children, 1967
- Assay of tyrosine transaminase activity by conversion of p-hydroxyphenylpyruvate to p-hydroxybenzaldehydeAnalytical Biochemistry, 1966