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Disease Info Card
Muscular Dystrophies, Limb-girdle
Information about Muscular Dystrophies, Limb-girdle: 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 Muscular Dystrophies, Limb-girdle
Most recent studies have shown that Muscular Dystrophies, Limb-girdle shares some biological mechanisms with atrophy, cardiomyopathies, cardiomyopathy-dilated, congenital-muscular-dystrophy-(disorder), distal-muscular-dystrophies, dystrophy, hypertrophy, leyden-moebius-muscular-dystrophy, miyoshi-myopathy, muscle-weakness, muscular-atrophy, muscular-dystrophy, muscular-dystrophy-duchenne, muscular-dystrophy-emery-dreifuss, myopathy, neuromuscular-diseases, sarcoglycanopathies, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Muscular Dystrophies, Limb-girdle, and have been seen in publications frequently: Aging, Autolysis, Cardiac Conduction, Cell Adhesion, Cell Death, Cell Differentiation, Glycosylation, Immune Response, Localization, Membrane Fusion, Muscle Atrophy, Muscle Contraction, Muscle Hypertrophy, Myoblast Fusion, Pathogenesis, Proteolysis, Regeneration, Reverse Transcription, Translation, Transport
Quite a number of genes have been found to play important roles in Muscular Dystrophies, Limb-girdle, such as CAPN3, CAV3, CHKA, DAG1, DMD, DYSF, FKRP, FKTN, LMNA, MYOT, SGCA, SGCB, SGCD, SGCG, TCAP, TRIM32, TTN. 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.