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Literature summary for 1.2.1.48 extracted from
- Sjoegren-Larsson syndrome: diversity of mutations and polymorphisms in the fatty aldehyde dehydrogenase gene (ALDH3A2) (2005), Hum. Mutat., 26, 1-10.
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Homo sapiens | - |
Sjoegren-Larsson syndrome is caused by mutations in the ALDH3A2 gene. Diversity of mutations and polymorphisms in the fatty aldehyde dehydrogenase gene ALDH3A2 | - |
Synonyms
| Synonyms | Comment | Organism |
|---|---|---|
| ALDH3A2 | - |
Homo sapiens |
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Release 2023.1 (January 2023)
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