Pub. Date : 2000 Jan
PMID : 10674710
1 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Hepatic methionine adenosyltransferase (MAT) deficiency is caused by mutations in the human MAT1A gene that abolish or reduce hepatic MAT activity that catalyzes the synthesis of S-adenosylmethionine from methionine and ATP. | S-Adenosylmethionine | methionine adenosyltransferase 1A | Homo sapiens |