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 …

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

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 …

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 …

Reading disabilities (RD) have a significant genetic basis and have shown linkage to
multiple regions including chromosome 15q. Dyslexia susceptibility 1 candidate gene 1 …

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 …

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

The status of DYX1C1 (C15q21. 3) as a susceptibility gene for dyslexia is unclear. We report
the association of this gene with reading and spelling ability in a sample of adolescent twins …

Abstract Recently, DYX1C1, a candidate gene for developmental dyslexia, encoding a
nuclear tetratricopepetide repeat domain protein dynamically regulated in brain, has been …