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Literature summary for 1.2.1.48 extracted from
- Sjoegren-Larsson syndrome: Molecular genetics and biochemical pathogenesis of fatty aldehyde dehydrogenase deficiency (2007), Mol. Genet. Metab., 90, 1-9.
Application
| Application | Comment | Organism |
|---|---|---|
| medicine | diagnosis and therapeutic approaches of Sjögren-Larsson syndrome | Homo sapiens |
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Homo sapiens | - |
Sjögren-Larsson syndrome is caused by mutations in the ALDH3A2 gene that codes for FALDH | - |
Synonyms
| Synonyms | Comment | Organism |
|---|---|---|
| ALDH3A2 | - |
Homo sapiens |
| ALDH3A2 | Sjögren-Larsson syndrome is caused by mutations in the ALDH3A2 gene that codes for FALDH | Homo sapiens |
| FALDH | - |
Homo sapiens |
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Release 2023.1 (January 2023)
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