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Mild to Moderate Intellectual Disability and Significant Speech and Language Deficits in Patients with FOXP1 Deletions and Mutations

Very recently, FOXP1 deficiency was shown to result in a phenotype of intellectual disability with significant speech and language impairment. Behavioral abnormalities should be considered as part of the clinical spectrum. Mild craniofacial abnormalities found in half of the described patients expan...

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Bibliografiske detaljer
Hovedforfatter: Horn, D.
Format: Artigo
Sprog:Inglês
Udgivet: S. Karger AG 2012
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3366708/
https://ncbi.nlm.nih.gov/pubmed/22670142
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000330916
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