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Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
Sequencing-based studies have identified novel risk genes associated with severe epilepsies and revealed an excess of rare deleterious variation in less-severe forms of epilepsy. To identify the shared and distinct ultra-rare genetic risk factors for different types of epilepsies, we performed a who...
Gardado en:
| Publicado en: | Am J Hum Genet |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Elsevier
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6698801/ https://ncbi.nlm.nih.gov/pubmed/31327507 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2019.05.020 |
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