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Prioritization of Epilepsy Associated Candidate Genes by Convergent Analysis
BACKGROUND: Epilepsy is a severe neurological disorder affecting a large number of individuals, yet the underlying genetic risk factors for epilepsy remain unclear. Recent studies have revealed several recurrent copy number variations (CNVs) that are more likely to be associated with epilepsy. The r...
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| Autori principali: | , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Public Library of Science
2011
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3044734/ https://ncbi.nlm.nih.gov/pubmed/21390307 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0017162 |
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