Prospective investigation of FOXP1 syndrome

Prospective investigation of FOXP1 syndrome

Abstract 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 d...

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Bibliographic Details
Main Authors: Paige M. Siper, Silvia De Rubeis, Maria del Pilar Trelles, Allison Durkin, Daniele Di Marino, François Muratet, Yitzchak Frank, Reymundo Lozano, Evan E. Eichler, Morgan Kelly, Jennifer Beighley, Jennifer Gerdts, Arianne S. Wallace, Heather C. Mefford, Raphael A. Bernier, Alexander Kolevzon, Joseph D. Buxbaum
Format: Article
Language:English
Published: BMC 2017-10-01
Series:Molecular Autism
Online Access:http://link.springer.com/article/10.1186/s13229-017-0172-6

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http://link.springer.com/article/10.1186/s13229-017-0172-6

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