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Disease Info Card
Muscle Eye Brain Disease
Information about Muscle Eye Brain Disease: 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 Muscle Eye Brain Disease
Most recent studies have shown that Muscle Eye Brain Disease shares some biological mechanisms with brain-diseases, congenital-anomaly-of-brain, congenital-muscular-dystrophy-(disorder), coronary-microvascular-disease, dysplasia, dystrophy, eye-abnormalities, fukuyama-type-congenital-muscular-dystrophy, hydrocephalus, hypoplasia, lissencephaly, muscle-hypotonia, muscular-dystrophies-limb-girdle, muscular-dystrophy, myopathy, nervousness, neuronal-migration-disorders, walker-warburg-congenital-muscular-dystrophy, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Muscle Eye Brain Disease, and have been seen in publications frequently: Basement Membrane Organization, Brain Development, Brain Morphogenesis, Cell Adhesion, Cell Differentiation, Eye Development, Fertilization, Forebrain Development, Glycosylation, Golgi Localization, Localization, Membrane Organization, Muscle Hypertrophy, Pathogenesis, Protein Folding, Protein Glycosylation, Rna Processing, Secretion, Signal Transmission, Tube Formation
Quite a number of genes have been found to play important roles in Muscle Eye Brain Disease, such as AGRN, CHKA, CHKB, DAG1, DMD, ERG, FKRP, FKTN, KCNH2, POMGNT1, POMT1, POMT2. 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.