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Disease Info Card
Developmental Reading Disorder
Information about Developmental Reading Disorder: 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 Developmental Reading Disorder
Most recent studies have shown that Developmental Reading Disorder shares some biological mechanisms with articulation-disorders, attention-deficit-hyperactivity-disorder, auditory-perceptual-disorders, autistic-disorder, basic-learning-problem-in-reading, cognition-disorders, developmental-disabilities, dyslexia, dyslexia-acquired, impairment-(finding), language-development-disorders, language-disorders, learning-disabilities, learning-disorders, malnutrition, nervous-system-disorder, perceptual-disorders, specific-language-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Developmental Reading Disorder, and have been seen in publications frequently: Axon Guidance, Brain Development, Clathrin-mediated Endocytosis, Cognition, Developmental Process, Localization, Long-term Memory, Myelination, Neurogenesis, Pathogenesis, Proprioception, Rna Interference, Segmentation, Sensory Perception, Sensory Processing, Short-term Memory, Translation, Transport, Transposition, Visual Perception
Quite a number of genes have been found to play important roles in Developmental Reading Disorder, such as AKR1C2, ATP2A2, DCDC2, EBPL, ELK3, ERMAP, EXOSC10, F2, FOXC2, KIAA0319, KIAA0319L, PEX7, PHYH, RAN, ROBO1. 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.