Disruptions of the _FOXP2_ gene cause a speech and language disorder involving difficulties in sequencing orofacial movements. FOXP2 is expressed in cortico-striatal and cortico-cerebellar circuits important for fine motor skills, and affected individuals show abnormalities in these brain regions. We selectively disrupted _Foxp2_ in the cerebellar Purkinje cells, striatum or cortex of mice and assessed the effects on skilled motor behaviour using an operant lever-pressing task. Foxp2 loss in each region impacted behaviour differently, with striatal and Purkinje cell disruptions affecting the variability and the speed of lever-press sequences, respectively. Mice lacking Foxp2 in Purkinje cells showed a prominent phenotype involving slowed le...
SummaryThe most well-described example of an inherited speech and language disorder is that observed...
FOXP2, the first gene to have been implicated in a developmental communication disorder, offers a un...
Mutations in the human FOXP2 gene cause impaired speech development and linguistic deficits, which h...
Disruptions of the FOXP2 gene cause a speech and language disorder involving difficulties in sequenc...
Mutations in the FOXP2 gene cause a severe neurodevelopmental speech and language disorder. In the K...
Mutations in the human FOXP2 gene cause impaired speech development and linguistic deficits, which h...
Disruptions of the FOXP2 gene cause a rare speech and language disorder, a discovery that has opened...
Disruption of FOXP2, a gene encoding a forkhead-domain transcription factor, causes a severe develop...
FOXP2 has been identified as a gene related to speech in humans, based on rare mutations that yield ...
Disruptions of the human FOXP2 gene cause problems with articulation of complex speech sounds, accom...
Heterozygous mutations of the human FOXP2 transcription factor gene cause the best-described example...
Heterozygous mutations of the Forkhead-box protein 2 (FOXP2) gene in humans cause childhood apraxia ...
It has been proposed that two amino acid substitutions in the transcription factor FOXP2 have been p...
We previously discovered that mutations of the human FOXP2 gene cause a monogenic communication diso...
The most well-described example of an inherited speech and language disorder is that observed in the...
SummaryThe most well-described example of an inherited speech and language disorder is that observed...
FOXP2, the first gene to have been implicated in a developmental communication disorder, offers a un...
Mutations in the human FOXP2 gene cause impaired speech development and linguistic deficits, which h...
Disruptions of the FOXP2 gene cause a speech and language disorder involving difficulties in sequenc...
Mutations in the FOXP2 gene cause a severe neurodevelopmental speech and language disorder. In the K...
Mutations in the human FOXP2 gene cause impaired speech development and linguistic deficits, which h...
Disruptions of the FOXP2 gene cause a rare speech and language disorder, a discovery that has opened...
Disruption of FOXP2, a gene encoding a forkhead-domain transcription factor, causes a severe develop...
FOXP2 has been identified as a gene related to speech in humans, based on rare mutations that yield ...
Disruptions of the human FOXP2 gene cause problems with articulation of complex speech sounds, accom...
Heterozygous mutations of the human FOXP2 transcription factor gene cause the best-described example...
Heterozygous mutations of the Forkhead-box protein 2 (FOXP2) gene in humans cause childhood apraxia ...
It has been proposed that two amino acid substitutions in the transcription factor FOXP2 have been p...
We previously discovered that mutations of the human FOXP2 gene cause a monogenic communication diso...
The most well-described example of an inherited speech and language disorder is that observed in the...
SummaryThe most well-described example of an inherited speech and language disorder is that observed...
FOXP2, the first gene to have been implicated in a developmental communication disorder, offers a un...
Mutations in the human FOXP2 gene cause impaired speech development and linguistic deficits, which h...