The signalling pathways controlling both the evolution and development of language in the
human brain remain unknown. So far, the transcription factor FOXP2 (forkhead box P2) is …

FOXP2 was the first gene shown to cause a Mendelian form of speech and language
disorder. Although developmentally expressed in many organs, loss of a single copy of …

FOXP2, the first gene causally linked to a human language disorder, is implicated in song
acquisition, production, and perception in oscine songbirds, the evolution of speech and …

Forkhead Box G1 (FOXG1) is a member of the Forkhead family of genes with non-redundant
roles in brain development, where alteration of this gene's expression significantly affects …

The FOXP2 transcription factor is one of the most well-known genes to have been implicated
in developmental speech and language disorders. Rare mutations disrupting the function of …

Foxp2 and Foxp1 are recently identified members of the Fox family of winged‐helix/forkhead
transcription factor genes. A recent study has found that mutations in human FOXP2 produce …

Foxp1 and Foxp2, which belong to the forkhead transcription factor family, are expressed in
the developing and adult mouse brain, including the striatum, thalamus, and cerebral cortex …

Mutations of FOXP2 are associated with altered brain structure, including the striatal part of
the basal ganglia, and cause a severe speech and language disorder. Songbirds serve as a …

A mutation of the forkhead box protein P2 (FOXP2) gene is associated with severe deficits in
human speech and language acquisition. In rodents, the humanized form of FOXP2 …

Genome-wide high-resolution array analysis is rapidly becoming a reliable method of
diagnostic investigation in individuals with mental retardation and congenital anomalies …