Disease Info Card

Language Disorders

Information about Language Disorders: 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 Language Disorders

Most recent studies have shown that Language Disorders shares some biological mechanisms with alzheimers-disease, aphasia, autistic-disorder, brain-injuries, cognition-disorders, communication-impairment, dementia, developmental-disabilities, dyslexia, epilepsy, hearing-problem, impairment-(finding), language-development-disorders, learning-disorders, malnutrition, memory-disorders, mental-disorders, specific-language-impairment, speech-disorders.

Among the many pathways, these few ones have gauged particular interests from scientists studying Language Disorders, and have been seen in publications frequently: Aging, Brain Development, Cell Adhesion, Cognition, Developmental Process, Localization, Long-term Memory, Myelination, Pathogenesis, Reflex, Segmentation, Sensory Processing, Short-term Memory, Social Behavior, Translation, Transport, Transposition, Visual Perception, Vocal Learning

Quite a number of genes have been found to play important roles in Language Disorders, such as ABR, BMP1, CNTNAP2, DLD, EBPL, ELK3, FAM3A, FMN1, FOXC2, FOXP2, GRN, LDHD, MAPT, RANGAP1, SHC2, SLC17A5, SLC6A3, TGM1. 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.

Language Disorders Related Genes

click to see detail information for each gene

ABR BMP1 CNTNAP2
DLD EBPL ELK3
FAM3A FMN1 FOXC2
FOXP2 GRN LDHD
MAPT RANGAP1 SHC2
SLC17A5 SLC6A3 TGM1