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Functional characterization of rare FOXP2 variants in neurodevelopmental disorder
BACKGROUND: Heterozygous disruption of FOXP2 causes a rare form of speech and language impairment. Screens of the FOXP2 sequence in individuals with speech/language-related disorders have identified several rare protein-altering variants, but their phenotypic relevance is often unclear. FOXP2 encode...
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| Publicado no: | J Neurodev Disord |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5126810/ https://ncbi.nlm.nih.gov/pubmed/27933109 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-016-9177-2 |
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