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Literature summary for 2.7.7.7 extracted from
- Mitochondrial DNA polymerase-gamma and human disease (2006), Hum. Mol. Genet., 15, R244-R252.
Application
| Application | Comment | Organism |
|---|---|---|
| medicine | clinically, POLG mutations can present from early neonatal life to late middle age, with a spectrum of phenotypes that includes common neurological disorders such as migraine, epilepsy and Parkinsonism | Homo sapiens |
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Homo sapiens | - |
- |
- |
Synonyms
| Synonyms | Comment | Organism |
|---|---|---|
| DNA polymerase gamma | - |
Homo sapiens |
| POLG | - |
Homo sapiens |
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Release 2023.1 (January 2023)
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