Developmental dyslexia is characterised by difficulties in learning to read. As reading is a
complex cognitive process, multiple genes are expected to contribute to the pathogenesis of …

Developmental dyslexia is a specific reading disability affecting children and adults who
otherwise possess normal intelligence, cognitive skills, and adequate schooling. Difficulties …

Dyslexia is a common heterogeneous disorder with a significant genetic component.
Multiple studies have replicated the evidence for linkage between variously defined …

Developmental dyslexia is a distinct learning disability with unexpected difficulty in learning
to read despite adequate intelligence, education, and environment, and normal senses. The …

Developmental dyslexia, or reading disability, is a multigenic complex disease for which at
least five loci, ie DYX1–3 and DYX5–6, have been clearly identified from the human …

Developmental dyslexia is a neurofunctional disorder characterised by an unexpected
difficulty in learning to read and write despite adequate intelligence, motivation, and …

A locus on chromosome 1p34-36 (DYX8) has been linked to developmental dyslexia or
reading disabilities (RD) in three independent samples. In the current study, we investigated …

We applied a family-based association approach to investigate the role of the DYX1C1 gene
on chromosome 15q as a candidate gene for developmental dyslexia (DD) to 158 families …

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 …

Dyslexia is the most common childhood learning disorder and it is a significantly heritable
trait. At least nine chromosomal loci have been linked to dyslexia, and additional …