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Disease Info Card
Leyden-moebius Muscular Dystrophy
Information about Leyden-moebius 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 Leyden-moebius Muscular Dystrophy
Most recent studies have shown that Leyden-moebius Muscular Dystrophy shares some biological mechanisms with atrophy, becker-muscular-dystrophy, distal-muscular-dystrophies, dystrophy, eosinophilic-myositis-(disorder), hereditary-diseases, miyoshi-myopathy, muscle-weakness, muscular-atrophy, muscular-dystrophies-limb-girdle, muscular-dystrophy, myopathy, myositis, neuromuscular-diseases, protein-deficiency, sarcoglycanopathies, severe-autosomal-recessive-muscular-dystrophy-of-childhood---north-african-type-(disorder), weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Leyden-moebius Muscular Dystrophy, and have been seen in publications frequently: Aging, Autolysis, Cell Adhesion, Cell Growth, Cell Proliferation, Localization, Mrna Splicing, Muscle Atrophy, Muscle Contraction, Muscle Hypertrophy, Myoblast Fusion, Pathogenesis, Proteolysis, Regeneration, Reverse Transcription, Rna Processing, Rna Splicing, Sex Determination, Translation
Quite a number of genes have been found to play important roles in Leyden-moebius Muscular Dystrophy, such as BRAF, CAPN2, CAPN3, CAV3, CHKA, CHKB, COG3, CSPG4, DMD, DYSF, FKRP, GNL3, IL32, KRAS, SGCA, SGCB, SGCG, TCAP, 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.