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Disease Info Card
Specific Language Impairment
Information about Specific Language Impairment: 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 Specific Language Impairment
Most recent studies have shown that Specific Language Impairment shares some biological mechanisms with articulation-disorders, attention-deficit-hyperactivity-disorder, auditory-perceptual-disorders, autism-spectrum-disorders, autistic-disorder, cognition-disorders, communication-impairment, developmental-disabilities, dyslexia, impairment-(finding), language-delays, language-development-disorders, language-disorders, learning-disorders, malnutrition, memory-disorders, pervasive-development-disorder, speech-disorders, tense.
Among the many pathways, these few ones have gauged particular interests from scientists studying Specific Language Impairment, and have been seen in publications frequently: Aging, Associative Learning, Brain Development, Cell Adhesion, Cognition, Developmental Process, Localization, Long-term Memory, Pathogenesis, Segmentation, Sensory Perception, Sensory Processing, Short-term Memory, Social Behavior, Translation, Visual Learning, Visual Perception
Quite a number of genes have been found to play important roles in Specific Language Impairment, such as ATP2C2, BMP1, CMIP, CNTNAP2, DHDDS, EBPL, ELK3, FOXP2, LDB1, NDP, PPFIBP1, SHC2, SULT1A3, SULT1A4, TGM1, ZACN. 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.