Glycogen Storage Disease Type Iii: Disease Bioinformatics
Research of Glycogen Storage Disease Type Iii has been linked to Glycogen Storage Disease, Storage Disease, Glycogen Storage Disease Type I, Myopathy, Hypoglycemia. The study of Glycogen Storage Disease Type Iii has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Glycogen Storage Disease Type Iii include Glycolysis, Excretion, Gluconeogenesis, Pathogenesis, Localization. These pathways complement our catalog of research reagents for the study of Glycogen Storage Disease Type Iii including antibodies and ELISA kits against ACID ALPHA-GLUCOSIDASE, AMYLO-1,6-GLUCOSIDASE, 4-ALPHA-GLUCANOTRANSFERASE, GROWTH HORMONE, AGL, ALB.
Top Research Reagents
We have 1874 products for the study of Glycogen Storage Disease Type Iii that can be applied to Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Glycogen Storage Disease Type Iii is also known as Gsd Iii, Limit Dextrinosis, Type Iii Glycogen Storage Disease, Amylo-1,6-glucosidase Deficiency, Cori Disease.