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Disease Info Card
Dyslexia
Information about Dyslexia: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Dyslexia
Most recent studies have shown that Dyslexia shares some biological mechanisms with agraphia, alexia, aphasia, articulation-disorders, attention-deficit-hyperactivity-disorder, autistic-disorder, basic-learning-problem-in-reading, brain-damage-chronic, cognition-disorders, developmental-disabilities, developmental-reading-disorder, dyslexia-acquired, impairment-(finding), language-development-disorders, language-disorders, learning-disabilities, learning-disorders, malnutrition, perceptual-disorders, speech-disorders.
Among the many pathways, these few ones have gauged particular interests from scientists studying Dyslexia, and have been seen in publications frequently: Aging, Brain Development, Cognition, Developmental Process, Localization, Long-term Memory, Myelination, Pathogenesis, Proprioception, Reflex, Rna Interference, Segmentation, Sensory Processing, Short-term Memory, Social Behavior, Translation, Transport, Transposition, Visual Learning, Visual Perception
Quite a number of genes have been found to play important roles in Dyslexia, such as ATP2A2, DCDC2, EBPL, ELK3, EP300, ERMAP, EXOSC10, FMN1, FOXC2, KIAA0319, PEX7, PHYH, PMEL, RAN, SLC10A3. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.