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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...
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| 發表在: | Epilepsia |
|---|---|
| Main Authors: | , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2014
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| 主題: | |
| 在線閱讀: | 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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