Article
Molecular phenotypes segregate missense mutations in SLC13A5 Epilepsy
medRxiv · 2024 · Jaramillo-Martinez, V.; Sennoune, S. R.; Tikhonova, E. B.; Karamyshev, A. L.; Ganapathy, V.; Urbatsch, I.
Key facts
| Title | Molecular phenotypes segregate missense mutations in SLC13A5 Epilepsy |
|---|---|
| First author | Jaramillo-Martinez, V.; Sennoune, S. R.; Tikhonova, E. B.; Karamyshev, A. L.; Ganapathy, V.; Urbatsch, I. |
| Journal | medRxiv |
| Published | Jan 1, 2024 |
| DOI | 10.1101/2024.05.23.594637 |
| Devices mentioned | K810863, K954191, K982485 |
| Product codes mentioned | DBM, LFZ, LXG, MVU |
At a glance
- 1–9 FDA submissions mentioned
- 1–9 Product codes mentioned
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About Literature
Peer-reviewed and preprint literature indexed by Orca1 and linked to the FDA submissions and product codes each article mentions. Only bibliographic details are shown here.
Source: Publisher and PubMed metadata; device mentions identified by Orca1