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...
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| Autores principales: | , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | inglés |
| Publicado: |
2014
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| Acceso en línea: | https://doi.org/10.1093/brain/awu206 https://academic.oup.com/brain/article-pdf/137/10/2680/17347758/awu206.pdf |
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