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Disease Info Card
Fukuyama Type Congenital Muscular Dystrophy
Information about Fukuyama Type 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 Fukuyama Type Congenital Muscular Dystrophy
Most recent studies have shown that Fukuyama Type Congenital Muscular Dystrophy shares some biological mechanisms with brain-diseases, congenital-anomaly-of-brain, congenital-muscular-dystrophy-(disorder), coronary-microvascular-disease, cortical-dysplasia, dysplasia, dystrophy, hydrocephalus, lissencephaly, muscle-eye-brain-disease, muscle-hypotonia, muscle-weakness, muscular-dystrophies-limb-girdle, muscular-dystrophy, muscular-dystrophy-duchenne, nervousness, polymicrogyria, walker-warburg-congenital-muscular-dystrophy, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Fukuyama Type Congenital Muscular Dystrophy, and have been seen in publications frequently: Aging, Brain Development, Cell Activation, Cell Adhesion, Cell Migration, Coagulation, Electron Transport, Fibrinolysis, Glycosylation, Lipid Storage, Localization, Membrane Organization, Myelination, Pathogenesis, Protein Glycosylation, Proteolysis, Reflex, Regeneration, Secretion, Transport
Quite a number of genes have been found to play important roles in Fukuyama Type Congenital Muscular Dystrophy, such as AGRN, CHKA, CHKB, DAG1, DCX, DMD, FKRP, FKTN, LAMA2, LMNA, POMGNT1, POMT1, POMT2, 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.