The role of common genetic variation in presumed monogenic epilepsies

BACKGROUND: The developmental and epileptic encephalopathies (DEEs) are the most severe group of epilepsies which co-present with developmental delay and intellectual disability (ID). DEEs usually occur in people without a family history of epilepsy and have emerged as primarily monogenic, with dama...

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Detalles Bibliográficos
Autores principales: Campbell, Ciarán, Leu, Costin, Feng, Yen-Chen Anne, Wolking, Stefan, Moreau, Claudia, Ellis, Colin, Ganesan, Shiva, Martins, Helena, Oliver, Karen, Boothman, Isabelle, Benson, Katherine, Molloy, Anne, Brody, Lawrence, Michaud, Jacques L., Hamdan, Fadi F., Minassian, Berge A., Lerche, Holger, Scheffer, Ingrid E., Sisodiya, Sanjay, Girard, Simon, Cosette, Patrick, Delanty, Norman, Lal, Dennis, Cavalleri, Gianpiero L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188960/
https://www.ncbi.nlm.nih.gov/pubmed/35679801
http://dx.doi.org/10.1016/j.ebiom.2022.104098

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188960/
https://www.ncbi.nlm.nih.gov/pubmed/35679801
http://dx.doi.org/10.1016/j.ebiom.2022.104098

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