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Rare variants and de novo variants in mesial temporal lobe epilepsy with hippocampal sclerosis
OBJECTIVE: We investigated the role of rare genetic variants and of de novo variants in the pathogenesis of mesial temporal lobe epilepsy related to hippocampal sclerosis (MTLE-HS). METHODS: Whole-exome sequencing (WES) was performed in patients with MTLE-HS and their unaffected parents (trios). Gen...
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| Publicado en: | Neurol Genet |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Wolters Kluwer
2018
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5999346/ https://ncbi.nlm.nih.gov/pubmed/29904720 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000245 |
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