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A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment
FOXP1 (forkhead box protein P1) is a transcription factor involved in the development of several tissues, including the brain. An emerging phenotype of patients with protein-disrupting FOXP1 variants includes global developmental delay, intellectual disability and mild to severe speech/language defi...
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| Publicado no: | Eur J Hum Genet |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4795189/ https://ncbi.nlm.nih.gov/pubmed/25853299 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2015.66 |
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