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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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| 出版年: | Epilepsia |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2014
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| 主題: | |
| オンライン･アクセス: | 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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