Chiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency

Human FOXP2 deficiency has been identified as a cause of hereditary developmental verbal dyspraxia. Another member of the same gene family, FOXP1, has expression patterns that overlap with FOXP2 in some areas of the brain, and FOXP1 and FOXP2 have the ability to form heterodimers. These findings sug...

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Detalhes bibliográficos
Main Authors: Carr, Christopher W, Moreno-De-Luca, Daniel, Parker, Colette, Zimmerman, Holly H, Ledbetter, Nikki, Martin, Christa Lese, Dobyns, William B, Abdul-Rahman, Omar A
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2987472/
https://ncbi.nlm.nih.gov/pubmed/20571508
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2010.96
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