Developmental dyslexia is a highly heritable disorder with a prevalence of at least 5% in
school-aged children. Linkage studies have identified numerous loci throughout the genome …

Developmental dyslexia (DD) is a complex neurodevelopmental deficit characterized by
impaired reading acquisition, in spite of adequate neurological and sensorial conditions …

DYX1C1 has been associated with dyslexia and neuronal migration in the develo**
neocortex. Unexpectedly, we found that deleting exons 2–4 of Dyx1c1 in mice caused a …

Dyslexia (or reading disability) and specific language impairment (or SLI) are common
childhood disorders that show considerable co-morbidity and diagnostic overlaps and have …

Dyslexia, or specific reading disability, is the most common learning disorder with a
complex, partially genetic basis, but its biochemical mechanisms remain poorly understood …

Dyslexia is a highly heritable learning disorder with a complex underlying genetic
architecture. Over the past decade, researchers have pinpointed a number of candidate …

BACKGROUND: Several susceptibility genes have been proposed for dyslexia (reading
disability; RD) and specific language impairment (SLI). RD and SLI show comorbidity, but it …

Dyslexia is among the most common neurodevelopmental disorders, with a prevalence of 5–
12%. At the phenotypic level, various cognitive components that enable reading and …

Several quantitative trait loci (QTLs) that influence developmental dyslexia (reading
disability [RD]) have been mapped to chromosome regions by linkage analysis. The most …

The human capacity to acquire complex language seems to be without parallel in the natural
world. The origins of this remarkable trait have long resisted adequate explanation, but …