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Disease Info Card
Learning Disabilities
Information about Learning Disabilities: 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 Learning Disabilities
Most recent studies have shown that Learning Disabilities shares some biological mechanisms with anxiety-disorders, attention-deficit-hyperactivity-disorder, autistic-disorder, child-behavior-disorders, cognition-disorders, depressive-disorder, developmental-disabilities, dyslexia, epilepsy, impairment-(finding), language-development-disorders, language-disorders, learning-disorders, malnutrition, mental-disorders, nervousness, neurofibromatoses, neurofibromatosis-1.
Among the many pathways, these few ones have gauged particular interests from scientists studying Learning Disabilities, and have been seen in publications frequently: Aging, Brain Development, Cell Death, Cognition, Localization, Long-term Memory, Mating, Methylation, Myelination, Neurogenesis, Pathogenesis, Reflex, Secretion, Segmentation, Short-term Memory, Social Behavior, Translation, Transport, Visual Perception
Quite a number of genes have been found to play important roles in Learning Disabilities, such as ARSA, CA1, DEGS1, ERMAP, FMN1, FMR1, FOXC2, MECP2, NF1, NHS, PEX7, PHYH, PMEL, SLC17A5, TBX1. 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.