Genetic disruptions of the forkhead box transcription factor FOXP2 in humans cause an
autosomal-dominant speech and language disorder. While FOXP2 expression pattern are …

FoxP2 is a highly conserved vertebrate transcription factor known for its importance in
human speech and language production. Disruption of FoxP2 in several vertebrate models …

Heterozygous mutations of the human FOXP2 gene cause a developmental disorder
involving impaired learning and production of fluent spoken language. Previous …

PURPOSE OF THE REVIEW: A reduced dosage of the transcription factor FOXP2 leads to
speech and language impairments probably owing to deficits in cortical and subcortical …

▪ Abstract A significant number of individuals have unexplained difficulties with acquiring
normal speech and language, despite adequate intelligence and environmental stimulation …

FOXP1 (forkhead box protein P1) is a transcription factor involved in the development of
several tissues, including the brain. An emerging phenotype of patients with protein …

This article gives an overview on the various brain structures, other than neocortex,
contributing to speech and language. The regions of the avian brain which are considered …

Forkhead domain transcription factors are a large gene family with multiple roles in
development. FOXP2, a recently identified member of this family, has been shown to be …

It has been suspected for several decades that genetic factors contribute to speech and
language development/function, based primarily on indirect data from twin studies and …

Plenty of animals can caw or roar or buzz, but only human beings can string a complex
series of sounds together into speech. Now a team of researchers has identified the first …