Describing the genetic architecture of epilepsy through heritability analysis

Epilepsy is a disease with substantial missing heritability; despite its high genetic component, genetic association studies have had limited success detecting common variants which influence susceptibility. In this paper, we reassess the role of common variants on epilepsy using extensions of herit...

Descripción completa

Detalles Bibliográficos
Autores principales: Speed, Doug, O’Brien, Terence J., Palotie, Aarno, Shkura, Kirill, Marson, Anthony G., Balding, David J., Johnson, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163034/
https://www.ncbi.nlm.nih.gov/pubmed/25063994
http://dx.doi.org/10.1093/brain/awu206

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163034/
https://www.ncbi.nlm.nih.gov/pubmed/25063994
http://dx.doi.org/10.1093/brain/awu206

Ejemplares similares