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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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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
S. Karger AG
2012
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| Online Zugang: | 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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