Pub. Date : 1993
PMID : 21290785
1 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Argininosuccinate Lyase Deficiency CLINICAL CHARACTERISTICS: Deficiency of argininosuccinate lyase (ASL), the enzyme that cleaves argininosuccinic acid to produce arginine and fumarate in the fourth step of the urea cycle, is characterized by a severe neonatal onset form and a late onset form. | Urea | argininosuccinate lyase | Homo sapiens |