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Disease Info Card
Merosin Deficient Congenital Muscular Dystrophy
Information about Merosin Deficient 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 Merosin Deficient Congenital Muscular Dystrophy
Most recent studies have shown that Merosin Deficient Congenital Muscular Dystrophy shares some biological mechanisms with congenital-muscular-dystrophy-(disorder), coronary-microvascular-disease, cortical-dysplasia, dysplasia, dystrophy, hypoplasia, muscle-contracture, muscle-eye-brain-disease, muscle-hypotonia, muscle-weakness, muscular-dystrophy, muscular-dystrophy-animal, muscular-dystrophy-duchenne, myopathy, nervousness, neuromuscular-diseases, peripheral-neuropathy, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Merosin Deficient Congenital Muscular Dystrophy, and have been seen in publications frequently: Cation Homeostasis, Cell Adhesion, Cell Differentiation, Cell Migration, Fertilization, Glomerular Filtration, Localization, Myelination, Nerve Development, Oligodendrocyte Differentiation, Pathogenesis, Reflex, Regeneration, Schwann Cell Differentiation, Schwann Cell Migration, Signal Transmission, Tissue Morphogenesis
Quite a number of genes have been found to play important roles in Merosin Deficient Congenital Muscular Dystrophy, such as CALB2, CD55, CR2, CSPG4, CTLA4, DAG1, DHRS4, DMD, FKTN, FN1, GDI1, GRIP1, HLA-DQA1, LAMA2, MITF, NOD2, TDGF1. 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.