Pub. Date : 2012 Jan-Feb
PMID : 22397046
2 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Sjogren-Larsson syndrome is an autosomal recessive neurocutaneous disease caused by mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, a microsomal enzyme that catalyzes the oxidation of medium- and long-chain aliphatic aldehydes fatty acids. | aliphatic aldehydes fatty acids | aldehyde dehydrogenase 3 family member A2 | Homo sapiens |
| 2 | Sjogren-Larsson syndrome is an autosomal recessive neurocutaneous disease caused by mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, a microsomal enzyme that catalyzes the oxidation of medium- and long-chain aliphatic aldehydes fatty acids. | aliphatic aldehydes fatty acids | aldehyde dehydrogenase 3 family member A2 | Homo sapiens |