l-Ornithine-ketoacid-transaminase deficiency in cultured fibroblasts of a patient with hyperornithinaemia and gyrate atrophy of the choroid and retina
- 1 September 1977
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 79 (2), 371-377
- https://doi.org/10.1016/0009-8981(77)90431-4
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- 144: Gyrate atrofy of the choroid and retina and ornithine-ketoacid aminotransferase deficiencyPediatric Research, 1976
- Genetic aspects in gyrate atrophy of the choroid and retina with hyperornithinaemia.British Journal of Ophthalmology, 1974
- Type 2 Hyperprolinemia: Absence of Δ 1 -Pyrroline-5-Carboxylic Acid Dehydrogenase ActivityScience, 1974
- Defective hydroxyproline metabolism in type II hyperprolinemiaBiochemical Medicine, 1974
- A radioisotopic assay for ornithine-δ-transaminaseAnalytical Biochemistry, 1973
- Ornithine-ketoacid transaminase activity in human skin and amniotic fluid cell cultureClinica Chimica Acta; International Journal of Clinical Chemistry, 1970
- Ornithinämie - eine weitere Aminosäurenstoffwechselstörung mit HirnschädigungDeutsche Medizinische Wochenschrift (1946), 1968
- PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENTJournal of Biological Chemistry, 1951