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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Detalles Bibliográficos
Autores principales: Estruch, Sara B., Graham, Sarah A., Chinnappa, Swathi M., Deriziotis, Pelagia, Fisher, Simon E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5126810/
https://www.ncbi.nlm.nih.gov/pubmed/27933109
http://dx.doi.org/10.1186/s11689-016-9177-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5126810/
https://www.ncbi.nlm.nih.gov/pubmed/27933109
http://dx.doi.org/10.1186/s11689-016-9177-2

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