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Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery
BACKGROUND: The relationship between monogenic and polygenic forms of epilepsy is poorly understood and the extent to which the genetic and acquired epilepsies share common pathways is unclear. Here, we use an integrated systems-level analysis of brain gene expression data to identify molecular netw...
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| Publicado no: | Genome Biol |
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| Main Authors: | , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5154105/ https://ncbi.nlm.nih.gov/pubmed/27955713 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13059-016-1097-7 |
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