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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Detalles Bibliográficos
Autores principales: Addis, Laura, Rosch, Richard E., Valentin, Antonio, Makoff, Andrew, Robinson, Robert, Everett, Kate V., Nashef, Lina, Pal, Deb K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830185/
https://www.ncbi.nlm.nih.gov/pubmed/27123475
http://dx.doi.org/10.1212/NXG.0000000000000056

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830185/
https://www.ncbi.nlm.nih.gov/pubmed/27123475
http://dx.doi.org/10.1212/NXG.0000000000000056

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