Language is a complex communicative behavior unique to humans, and its genetic basis is poorly understood. Genes associated with human speech and language disorders provide some insights, originating with the FOXP2 transcription factor, a mutation in which is the source of an inherited form of developmental verbal dyspraxia. Subsequently, targets of FOXP2 regulation have been associated with speech and language disorders, along with other genes. Here, we review these recent findings that implicate genetic factors in human speech. Due to the exclusivity of language to humans, no single animal model is sufficient to study the complete behavioral effects of these genes. Fortunately, some animals possess subcomponents of language. One such subc...
In 2001, a point mutation in the forkhead box P2 (FOXP2) coding sequence was identified as the basis...
It is well known that FOXP2 has a connection to human language. In a familial case study of humans i...
In 2001, a point mutation in the forkhead box P2 (FOXP2) coding sequence was identified as the basis...
Language is a complex communicative behavior unique to humans, and its genetic basis is poorly under...
Language is a complex communicative behavior unique to humans, and its genetic basis is poorly under...
The mysterious human propensity for acquiring speech and language has fascinated sci-entists for dec...
The mysterious human propensity for acquiring speech and language has fascinated scientists for deca...
Vocal learning is a rare trait. Humans depend on vocal learning to acquire spoken language, but most...
Vocal learning is a rare trait. Humans depend on vocal learning to acquire spoken language, but most...
Vocal learning is a rare trait. Humans depend on vocal learning to acquire spoken language, but most...
Language is a complex communicative behavior unique to humans, though its genetic basis is still poo...
Disorders of speech and language are highly heritable, providing strong support for a genetic basis....
Disorders of speech and language are highly heritable, providing strong support for a genetic basis....
Disorders of speech and language are highly heritable, providing strong support for a genetic basis....
The mysterious human propensity for acquiring speech and language has fascinated scientists for deca...
In 2001, a point mutation in the forkhead box P2 (FOXP2) coding sequence was identified as the basis...
It is well known that FOXP2 has a connection to human language. In a familial case study of humans i...
In 2001, a point mutation in the forkhead box P2 (FOXP2) coding sequence was identified as the basis...
Language is a complex communicative behavior unique to humans, and its genetic basis is poorly under...
Language is a complex communicative behavior unique to humans, and its genetic basis is poorly under...
The mysterious human propensity for acquiring speech and language has fascinated sci-entists for dec...
The mysterious human propensity for acquiring speech and language has fascinated scientists for deca...
Vocal learning is a rare trait. Humans depend on vocal learning to acquire spoken language, but most...
Vocal learning is a rare trait. Humans depend on vocal learning to acquire spoken language, but most...
Vocal learning is a rare trait. Humans depend on vocal learning to acquire spoken language, but most...
Language is a complex communicative behavior unique to humans, though its genetic basis is still poo...
Disorders of speech and language are highly heritable, providing strong support for a genetic basis....
Disorders of speech and language are highly heritable, providing strong support for a genetic basis....
Disorders of speech and language are highly heritable, providing strong support for a genetic basis....
The mysterious human propensity for acquiring speech and language has fascinated scientists for deca...
In 2001, a point mutation in the forkhead box P2 (FOXP2) coding sequence was identified as the basis...
It is well known that FOXP2 has a connection to human language. In a familial case study of humans i...
In 2001, a point mutation in the forkhead box P2 (FOXP2) coding sequence was identified as the basis...