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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Detaylı Bibliyografya
Yayımlandı:Epilepsia
Asıl Yazarlar: Seltzer, Laurie E., Ma, Mandy, Ahmed, Sohnee, Bertrand, Mary, Dobyns, William B., Wheless, James, Paciorkowski, Alex R.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2014
Konular:
Article
Online Erişim: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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