The capacity for language is one of the key features underlying the complexity of human cognition and its evolution. However, little is known about the neurobiological mechanisms that mediate normal or impaired linguistic ability. For developmental dyslexia, early postmortem studies conducted in the 1980s linked the disorder to subtle defects in the migration of neurons in the developing neocortex. These early studies were reinforced by human genetic analyses that identified dyslexia susceptibility genes and subsequent evidence of their involvement in neuronal migration. In this review, we examine recent experimental evidence that does not support the link between dyslexia and neuronal migration. We critically evaluate gene function studies...
Dyslexia is among the most common neurodevelopmental disorders, with a prevalence of 5–12%. At the ...
Developmental dyslexia is a common disorder with a strong genetic component, but the underlying mole...
Developmental dyslexia is a common disorder with a strong genetic component, but the underlying mole...
The capacity for language is one of the key features underlying the complexity of human cognition an...
The capacity for language is one of the key features underlying the complexity of human cognition an...
The capacity for language is one of the key features underlying the complexity of human cognition an...
The capacity for language is one of the key features underlying the complexity of human cognition an...
The capacity for language is one of the key features underlying the complexity of human cognition an...
The capacity for language is one of the key features underlying the complexity of human cognition an...
This work was supported by the Wellcome Trust (092071/Z/10/Z to A.P.M., Z.M. and A.V.-B., and 082498...
Linkage analysis has revealed a number of gene intervals conferring susceptibility to developmental ...
Linkage analysis has revealed a number of gene intervals conferring susceptibility to developmental ...
Abstract—Rodent homologues of two candidate dyslexia susceptibility genes, Kiaa0319 and Dcdc2, have ...
The development of the brain is an immensely complicated process that is highly regulated by numerou...
The development of the brain is an immensely complicated process that is highly regulated by numerou...
Dyslexia is among the most common neurodevelopmental disorders, with a prevalence of 5–12%. At the ...
Developmental dyslexia is a common disorder with a strong genetic component, but the underlying mole...
Developmental dyslexia is a common disorder with a strong genetic component, but the underlying mole...
The capacity for language is one of the key features underlying the complexity of human cognition an...
The capacity for language is one of the key features underlying the complexity of human cognition an...
The capacity for language is one of the key features underlying the complexity of human cognition an...
The capacity for language is one of the key features underlying the complexity of human cognition an...
The capacity for language is one of the key features underlying the complexity of human cognition an...
The capacity for language is one of the key features underlying the complexity of human cognition an...
This work was supported by the Wellcome Trust (092071/Z/10/Z to A.P.M., Z.M. and A.V.-B., and 082498...
Linkage analysis has revealed a number of gene intervals conferring susceptibility to developmental ...
Linkage analysis has revealed a number of gene intervals conferring susceptibility to developmental ...
Abstract—Rodent homologues of two candidate dyslexia susceptibility genes, Kiaa0319 and Dcdc2, have ...
The development of the brain is an immensely complicated process that is highly regulated by numerou...
The development of the brain is an immensely complicated process that is highly regulated by numerou...
Dyslexia is among the most common neurodevelopmental disorders, with a prevalence of 5–12%. At the ...
Developmental dyslexia is a common disorder with a strong genetic component, but the underlying mole...
Developmental dyslexia is a common disorder with a strong genetic component, but the underlying mole...