Prospective investigation of FOXP1 syndrome

BACKGROUND: Haploinsufficiency of the forkhead-box protein P1 (FOXP1) gene leads to a neurodevelopmental disorder termed FOXP1 syndrome. Previous studies in individuals carrying FOXP1 mutations and deletions have described the presence of autism spectrum disorder (ASD) traits, intellectual disabilit...

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Detalles Bibliográficos
Autores principales: Siper, Paige M., De Rubeis, Silvia, Trelles, Maria del Pilar, Durkin, Allison, Di Marino, Daniele, Muratet, François, Frank, Yitzchak, Lozano, Reymundo, Eichler, Evan E., Kelly, Morgan, Beighley, Jennifer, Gerdts, Jennifer, Wallace, Arianne S., Mefford, Heather C., Bernier, Raphael A., Kolevzon, Alexander, Buxbaum, Joseph D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655854/
https://www.ncbi.nlm.nih.gov/pubmed/29090079
http://dx.doi.org/10.1186/s13229-017-0172-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655854/
https://www.ncbi.nlm.nih.gov/pubmed/29090079
http://dx.doi.org/10.1186/s13229-017-0172-6

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