Foxp subfamily genes were recently recognized to be members of the Fox gene family. Foxp
subfamily members contain a zinc finger domain and a leucine zipper motif in addition to a …

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 …

Disruption of FOXP2, a gene encoding a forkhead‐domain transcription factor, causes a
severe developmental disorder of verbal communication, involving profound articulation …

De novo disruptions of the neural transcription factor FOXP1 are a recently discovered, rare
cause of sporadic intellectual disability (ID). We report three new cases of FOXP1-related …

FOXP2 is a forkhead transcription factor implicated in developmental verbal dyspraxia, a
human speech and language disorder. FOXP2 is expressed in complex patterns during …

Many members of the forkhead/winged helix transcriptional factors are known to be
regulators of embryogenesis. Mutations of the Fox gene family have been implicated in a …

Mutations in FOXP2, a member of the forkhead family of transcription factor genes, are the
only known cause of developmental speech and language disorders in humans. To date …

Background Heterozygous disruption of FOXP2 causes a rare form of speech and language
impairment. Screens of the FOXP2 sequence in individuals with speech/language-related …

FOXP transcription factors are an evolutionarily ancient protein subfamily coordinating the
development of several organ systems in the vertebrate body. Association of their genes …

FOXP2, the first gene to have been implicated in a developmental communication disorder,
offers a unique entry point into neuromolecular mechanisms influencing human speech and …