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Epilepsy and outcome in FOXG1-related disorders
OBJECTIVE: FOXG1-related disorders are associated with severe intellectual disability, absent speech with autistic features, and epilepsy. Children with deletions or intragenic mutations of FOXG1 also have postnatal microcephaly, morphologic abnormalities of the corpus callosum, and choreiform movem...
Gardado en:
| Publicado en: | Epilepsia |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2014
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4265461/ https://ncbi.nlm.nih.gov/pubmed/24836831 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/epi.12648 |
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