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Chipping away at the common epilepsies with complex genetics: the 15q13.3 microdeletion shows the way
The idiopathic epilepsies are genetically heterogeneous with more than 50 clinical classifications. They are characterized by episodic seizures arising from erratic neuronal discharge in susceptible individuals. The most common predisposing genetic cause is the recently discovered chromosome 15q13.3...
| Autores principales: | , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2009
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2664944/ https://www.ncbi.nlm.nih.gov/pubmed/19341504 http://dx.doi.org/10.1186/gm33 |