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Gene panel analysis for nonsyndromic cryptogenic neonatal/infantile epileptic encephalopathy
OBJECTIVE: Epileptic encephalopathy (EE) is a heterogeneous condition associated with deteriorations of cognitive, sensory and/or motor functions as a consequence of epileptic activity. The phenomenon is the most common and severe in infancy and early childhood. Genetic‐based diagnosis in EE patient...
Tallennettuna:
| Julkaisussa: | Epilepsia Open |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
John Wiley and Sons Inc.
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5719849/ https://ncbi.nlm.nih.gov/pubmed/29588952 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/epi4.12055 |
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