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A Novel SCN1A Mutation: A Case Report
INTRODUCTION: Dravet syndrome (DS) is characterized by severe infant-onset myoclonic epilepsy with delayed psychomotor development and increased premature mortality. The seizures triggered by fire have been gradually decreased over time, and finally they start to occur without fever at the age of 2–...
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| Publicado no: | J Pediatr Neurosci |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer - Medknow
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7519752/ https://ncbi.nlm.nih.gov/pubmed/33042244 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/jpn.JPN_118_18 |
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