A novel variant of unknown significance in pediatric epilepsy: a case report
Variants in SCN8A are associated with several diseases, including developmental and epileptic encephalopathy, intermediate epilepsy or mild-to-moderate developmental and epileptic encephalopathy, self-limited familial infantile epilepsy, neurodevelopmental delays with generalized epilepsy, neurodeve...
Tallennettuna:
| Päätekijät: | , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
SAGE Publishing
2023-07-01
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| Sarja: | Journal of International Medical Research |
| Linkit: | https://doi.org/10.1177/03000605231187931 |
| Tagit: |
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