Pub. Date : 2018
PMID : 28980192
1 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | BACKGROUND: Very long chain acyl CoA dehydrogenase (VLCAD) deficiency (OMIM#201475) is an autosomal recessive disorder of fatty acid beta oxidation caused by defect in the ACADVL. | Fatty Acids | acyl-CoA dehydrogenase very long chain | Homo sapiens |