SummaryMutation of the DNA-binding region of the FOXP2 protein causes an inherited language disorder. A recent study provides the first data on mice with this mutation, which exhibit deficits in motor-skill learning and abnormal properties of neural circuits that contribute to these skills
Childhood syndromes disturbing language development are common and display high degrees of heritabil...
Childhood syndromes disturbing language development are common and display high degrees of heritabil...
Disruptions of the FOXP2 gene cause a rare speech and language disorder, a discovery that has opened...
Heterozygous mutations of the human FOXP2 transcription factor gene cause the best-described example...
Heterozygous mutations of the human FOXP2 transcription factor gene cause the best-described example...
Mutations in the FOXP2 gene cause a severe neurodevelopmental speech and language disorder. In the K...
SummaryThe most well-described example of an inherited speech and language disorder is that observed...
The most well-described example of an inherited speech and language disorder is that observed in the...
Mutations in the human FOXP2 gene cause impaired speech development and linguistic deficits, which h...
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...
FOXP2, the first gene to have been implicated in a developmental communication disorder, offers a un...
FOXP2, the first gene to have been implicated in a developmental communication disorder, offers a un...
FOXP2, the first gene to have been implicated in a developmental communication disorder, offers a un...
Rare mutations of the FOXP2 transcription factor gene cause a monogenic syndrome characterized by im...
Childhood syndromes disturbing language development are common and display high degrees of heritabil...
Childhood syndromes disturbing language development are common and display high degrees of heritabil...
Disruptions of the FOXP2 gene cause a rare speech and language disorder, a discovery that has opened...
Heterozygous mutations of the human FOXP2 transcription factor gene cause the best-described example...
Heterozygous mutations of the human FOXP2 transcription factor gene cause the best-described example...
Mutations in the FOXP2 gene cause a severe neurodevelopmental speech and language disorder. In the K...
SummaryThe most well-described example of an inherited speech and language disorder is that observed...
The most well-described example of an inherited speech and language disorder is that observed in the...
Mutations in the human FOXP2 gene cause impaired speech development and linguistic deficits, which h...
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...
FOXP2, the first gene to have been implicated in a developmental communication disorder, offers a un...
FOXP2, the first gene to have been implicated in a developmental communication disorder, offers a un...
FOXP2, the first gene to have been implicated in a developmental communication disorder, offers a un...
Rare mutations of the FOXP2 transcription factor gene cause a monogenic syndrome characterized by im...
Childhood syndromes disturbing language development are common and display high degrees of heritabil...
Childhood syndromes disturbing language development are common and display high degrees of heritabil...
Disruptions of the FOXP2 gene cause a rare speech and language disorder, a discovery that has opened...
DOI
Add to ORKG