Embryonic knockdown of candidate dyslexia susceptibility gene (CDSG) homologs in
cerebral cortical progenitor cells in the rat results in acute disturbances of neocortical …

INTRODUCTION: Dyslexia is a learning disability in which reading (but not any other)
impairment is the most prominent symptom. There seems to be a high comorbidity among …

Substantial heritability has been reported for developmental dyslexia (DD), and KIAA0319
and ROBO1 appear as more than plausible candidate susceptibility genes for this …

Within the last decade several genes have been identified as candidate risk genes for
developmental dyslexia. Recent research using animal models and embryonic RNA …

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 …

Dyslexia is a common pediatric disorder that affects 5–17% of schoolchildren in the United
States. It is marked by unexpected difficulties in fluent reading despite adequate intelligence …

Background Developmental dyslexia (DD) and attention deficit/hyperactivity disorder
(ADHD) are among the most common neurodevelopmental disorders, whose etiology …

DYX1C1 was first identified as a candidate gene for dyslexia susceptibility, and its role in
controlling neuronal migration during embryogenesis and effect on learning in rodents have …

Objective Dyslexia-susceptibility-1-candidate-1 (DYX1C1) was the first gene associated with
dyslexia. Since the original report of 2003, eight replication attempts have been published …

Cytoplasmic assembly of ciliary dyneins, a process known as preassembly, requires
numerous non-dynein proteins, but the identities and functions of these proteins are not fully …