Research of Walker-warburg Congenital Muscular Dystrophy has been linked to Muscular Dystrophy, Dystrophy, Congenital Muscular Dystrophy (disorder), Eye Abnormalities, Lissencephaly. The study of Walker-warburg Congenital Muscular Dystrophy has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Walker-warburg Congenital Muscular Dystrophy include Glycosylation, Pathogenesis, Localization, Protein Glycosylation, Myelination. These pathways complement our catalog of research reagents for the study of Walker-warburg Congenital Muscular Dystrophy including antibodies and ELISA kits against FKTN, POMGNT1, FKRP, POMT1, ALPHA-DYSTROGLYCAN.
Top Research Reagents
We have 916 products for the study of Walker-warburg Congenital Muscular Dystrophy that can be applied to Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Walker-warburg Congenital Muscular Dystrophy is also known as Chemke Syndrome, Syndrome, Chemke, Syndrome, Walker-warburg, Walker Warburg Syndrome, Walker-warburg Syndrome.