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Disease Info Card
Walker-warburg Congenital Muscular Dystrophy
Information about Walker-warburg Congenital Muscular Dystrophy: 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 Walker-warburg Congenital Muscular Dystrophy
Most recent studies have shown that Walker-warburg Congenital Muscular Dystrophy shares some biological mechanisms with brain-diseases, cobblestone-lissencephaly, congenital-abnormality, congenital-anomaly-of-brain, congenital-cerebral-hernia, congenital-muscular-dystrophy-(disorder), coronary-microvascular-disease, dysplasia, dystrophy, eye-abnormalities, fukuyama-type-congenital-muscular-dystrophy, hydrocephalus, hypoplasia, lissencephaly, muscle-eye-brain-disease, muscle-hypotonia, muscular-dystrophies-limb-girdle, muscular-dystrophy, nervousness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Walker-warburg Congenital Muscular Dystrophy, and have been seen in publications frequently: Aging, Brain Development, Cell Adhesion, Cell Migration, Developmental Process, Fermentation, Fertilization, Glycosylation, Golgi Localization, Lactation, Localization, Membrane Organization, Myelination, Neural Tube Closure, Neurogenesis, Pathogenesis, Protein Glycosylation, Rna Interference, Secretion, Virulence
Quite a number of genes have been found to play important roles in Walker-warburg Congenital Muscular Dystrophy, such as AGRN, CHKA, CHKB, DAG1, DMD, FKRP, FKTN, POMGNT1, POMT1, POMT2, SGCA, VIM. 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.