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Analysis of rare copy number variation in absence epilepsies
OBJECTIVE: To identify shared genes and pathways between common absence epilepsy (AE) subtypes (childhood absence epilepsy [CAE], juvenile absence epilepsy [JAE], and unclassified absence epilepsy [UAE]) that may indicate common mechanisms for absence seizure generation and potentially a diagnostic...
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| Veröffentlicht in: | Neurol Genet |
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| Hauptverfasser: | , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Wolters Kluwer
2016
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4830185/ https://ncbi.nlm.nih.gov/pubmed/27123475 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000056 |
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