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Spectrum of SCN8A-Related Epilepsy
Investigators from the EuroEPINOMICS European research consortium studied 17 patients with epileptic encephalopathy due to SCN8A mutations and reported the specific genetic and phenotypic features.
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| Udgivet i: | Pediatr Neurol Briefs |
|---|---|
| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Pediatric Neurology Briefs Publishers
2015
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4747291/ https://ncbi.nlm.nih.gov/pubmed/26933559 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15844/pedneurbriefs-29-2-7 |
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