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Origins of Epilepsy in Fragile X Syndrome
Fragile X syndrome is the leading heritable form of cognitive impairment and the leading known monogenic disorder associated with autism. Roughly one-quarter of children with this disorder have seizures, most of which are relatively benign and are resolved beyond childhood. Because of the prevalence...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Science Inc
2009
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2728488/ https://ncbi.nlm.nih.gov/pubmed/19693328 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1535-7511.2009.01309.x |
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