Defective ornithine metabolism in the syndrome of hyperornithinaemia, hyperammonaemia and homocitrullinuria
- 1 December 1981
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 4 (1) , 95-96
- https://doi.org/10.1007/bf02263608
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- METABOLIC DEFECT IN HYPERORNITHINÆMIAThe Lancet, 1974
- Ornithine-ketoacid transaminase activity in human skin and amniotic fluid cell cultureClinica Chimica Acta; International Journal of Clinical Chemistry, 1970
- Hyperornithinemia, Hyperammonemia, and HomocitrullinuriaAmerican Journal of Diseases of Children, 1969
- Ornithinämie - eine weitere Aminosäurenstoffwechselstörung mit HirnschädigungDeutsche Medizinische Wochenschrift (1946), 1968