Research of Mucopolysaccharidosis Iii has been linked to Mucopolysaccharidoses, Mps Iii A, Mucopolysaccharidosis Type Iiib, Lysosomal Storage Diseases, Mucopolysaccharidosis I. The study of Mucopolysaccharidosis Iii has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Mucopolysaccharidosis Iii include Excretion, Pathogenesis, Transport, Glycosylation, Secretion. These pathways complement our catalog of research reagents for the study of Mucopolysaccharidosis Iii including antibodies and ELISA kits against SGSH, NAGLU, MAP3K14, HGSNAT, ARSH.
Mucopolysaccharidosis Iii 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 Mucopolysaccharidosis Iii below!
For more information on how to use Laverne, please read the How to Guide.
We have 640 products for the study of Mucopolysaccharidosis Iii that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Mucopolysaccharidosis Iii is also known as mucopolysaccharidosis iii, mucopolysaccharidosis type iiia, mucopolysaccharidosis type iiib, mucopolysaccharidosis type iii, sanfilippo syndrome a, sanfilippo syndrome, n-acetyl-alpha-d-glucosaminidase deficiency, n-sulphoglucosamine sulphohydrolase deficiency, mucopolysaccharidosis, mps-iii-b (disorder), mucopoly-saccharidosis type 3b, mucopoly-saccharidosis type 3a, mucopolysaccharidosis, mps-iii, mucopoly-saccharidosis type 3, mucopolysaccharidoses, sanfilippo's syndrome, sanfilippos syndrome, naglu deficiency, mps iii a, mps iii, mps 3a, mps 3b.
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