Research of Myotonic Dystrophy has been linked to Dystrophy, Muscular Dystrophy, Myopathy, Neuromuscular Diseases, Atrophy. The study of Myotonic Dystrophy has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Myotonic Dystrophy include Pathogenesis, Localization, Cardiac Conduction, Secretion, Translation. These pathways complement our catalog of research reagents for the study of Myotonic Dystrophy including antibodies and ELISA kits against DMPK, CNBP, MBNL1, CELF1, INS.
Myotonic Dystrophy Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Myotonic Dystrophy below!
For more information on how to use Laverne, please read the How to Guide.
We have 1518 products for the study of Myotonic Dystrophy that can be applied to Western Blot, Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Myotonic Dystrophy is also known as myotonic dystrophy, dystrophia myotonica, myotonia dystrophica, steinert myotonic dystrophy syndrome (disorder), steinert myotonic dystrophy syndrome, curschmann-batten-steinert syndrome, steinert's disease, steinert disease.
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