Ornithine transcarbamylase, an isoelectric point (pI) isozyme in human liver and its deficiency
- 1 October 1971
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 45 (1) , 145-150
- https://doi.org/10.1016/0006-291x(71)90062-3
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Periodic attacks of lethargy in a baby with ammonia intoxication due to a congenital defect in ureogenesis.Archives of Disease in Childhood, 1969
- Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase.Archives of Disease in Childhood, 1969
- Studies on extracellular proteins from Staphylococcus aureusBiochimica et Biophysica Acta (BBA) - Protein Structure, 1967
- Comparative Biochemistry of Urea SynthesisPublished by Elsevier ,1959