Wird geladen...
Novel SZT2 mutations in three patients with developmental and epileptic encephalopathies
BACKGROUND: The seizure threshold 2 (SZT2) gene encodes a large, highly conserved protein that lowers seizure threshold and may also enhance epileptogenesis. In this study, three patients diagnosed with SZT2‐related developmental and epileptic encephalopathies (DEEs) were reviewed aiming to expand k...
Gespeichert in:
| Veröffentlicht in: | Mol Genet Genomic Med |
|---|---|
| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
John Wiley and Sons Inc.
2019
|
| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6732301/ https://ncbi.nlm.nih.gov/pubmed/31397114 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.926 |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|