Already since the earliest endeavors to study the brain, researchers have been fascinated
by how activity in the brain enables us to interact with the world around us. For example …

Already since the earliest endeavors to study the brain, researchers have been fascinated
by how activity in the brain enables us to interact with the world around us. For example …

Human speech and language are among the most complex motor and cognitive abilities.
The discovery of a mutation in the transcription factor FOXP2 in KE family members with …

FOXP2 was the first identified monogenic cause of a speech disorder (for review see
Graham et al., 2015). However, it remains to be answered how it affects the development of …

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

Rare disruptions of FOXP2 have been strongly implicated in deficits in language
development. Research over the past decade has suggested a role in the formation of …

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 …

Aim To delineate the speech and language phenotype of a cohort of individuals with FOXP1‐
related disorder. Method We administered a standardized test battery to examine speech …

Motivation Heterozygous mutations of the transcription factor FOXP2 in humans lead to
childhood apraxia of speech. FOXP2 is highly expressed in GABAergic and dopaminergic …

Heterozygous mutations of the transcription factor FOXP2 in humans lead to childhood
apraxia of speech (CAS). FOXP2 is highly expressed in GABAergic and dopaminergic …