Prospective investigation of FOXP1 syndrome
Prospective investigation of FOXP1 syndrome
About this item
Full title
Author / Creator
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 and Buxbaum, Joseph D.
Publisher
England: BioMed Central Ltd
Journal title
Language
English
Formats
Publication information
Publisher
England: BioMed Central Ltd
Subjects
More information
Scope and Contents
Contents
Haploinsufficiency of the forkhead-box protein P1 (
) gene leads to a neurodevelopmental disorder termed FOXP1 syndrome. Previous studies in individuals carrying
mutations and deletions have described the presence of autism spectrum disorder (ASD) traits, intellectual disability, language impairment, and psychiatric features. The goal of the...
Alternative Titles
Full title
Prospective investigation of FOXP1 syndrome
Authors, Artists and Contributors
Author / Creator
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.
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_0b5ffff4126d4a909fb049f2338f379d
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_0b5ffff4126d4a909fb049f2338f379d
Other Identifiers
ISSN
2040-2392
E-ISSN
2040-2392
DOI
10.1186/s13229-017-0172-6
