Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy

Because hyper-excitability has been shown to be a shared pathophysiological mechanism, we used the latest and largest genome-wide studies in amyotrophic lateral sclerosis (n = 36,052) and epilepsy (n = 38,349) to determine genetic overlap between these conditions. First, we showed no significant gen...

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Detalles Bibliográficos
Autores principales: Schijven, Dick, Stevelink, Remi, McCormack, Mark, van Rheenen, Wouter, Luykx, Jurjen J., Koeleman, Bobby P.C., Veldink, Jan H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818383/
https://www.ncbi.nlm.nih.gov/pubmed/32409253
http://dx.doi.org/10.1016/j.neurobiolaging.2020.04.011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818383/
https://www.ncbi.nlm.nih.gov/pubmed/32409253
http://dx.doi.org/10.1016/j.neurobiolaging.2020.04.011

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