Foxp1 expression is essential for sex-specific murine neonatal ultrasonic vocalization

Abstract. Autism and speech and language deficits are predominantly found in boys, however the causative mechanisms for this sex bias are unknown. Human FOXP1

Saved in:
Bibliographic Details
Main Authors: Fröhlich, Henning (Author) , Rafiullah, Rafiullah (Author) , Abele, Sonja (Author) , Rappold, Gudrun (Author)
Format: Article (Journal)
Language:English
Published: [15 April 2017]
In: Human molecular genetics
Year: 2017, Volume: 26, Issue: 8, Pages: 1511-1521
ISSN:1460-2083
DOI:10.1093/hmg/ddx055
Online Access:Verlag, Volltext: http://dx.doi.org/10.1093/hmg/ddx055
Verlag, Volltext: https://academic.oup.com/hmg/article/26/8/1511/2997574
Get full text
Author Notes:Henning Fröhlich, Rafiullah Rafiullah, Nathalie Schmitt, Sonja Abele and Gudrun A. Rappold
Description
Summary:Abstract. Autism and speech and language deficits are predominantly found in boys, however the causative mechanisms for this sex bias are unknown. Human FOXP1
Item Description:Gesehen am 25.05.2018
Physical Description:Online Resource
ISSN:1460-2083
DOI:10.1093/hmg/ddx055