Molecular cloning and nucleotide sequence of cDNA for human liver arginase.
Arginase (EC 3.5.3.1) catalyzes the last step of the urea cycle in the liver of ureotelic animals. Inherited deficiency of the enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia. To facilitate investigation of the enzyme and gene structures and to elucidat...
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| Publicat a: | Proc Natl Acad Sci U S A |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
1987
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC304217/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3540966/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.84.2.412 |
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