Research of Mucopolysaccharidosis Vi has been linked to Mucopolysaccharidoses, Lysosomal Storage Diseases, Mucopolysaccharidosis I, Mucopolysaccharidosis Iv, Mucopolysaccharidosis Ii. The study of Mucopolysaccharidosis Vi has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Mucopolysaccharidosis Vi include Excretion, Localization, Ossification, Transport, Hypersensitivity. These pathways complement our catalog of research reagents for the study of Mucopolysaccharidosis Vi including antibodies and ELISA kits against ALPHA-L-IDURONIDASE, ALAS2, ARSA, ARSB, CAT.
Mucopolysaccharidosis Vi 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 Vi below!
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We have 938 products for the study of Mucopolysaccharidosis Vi that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Mucopolysaccharidosis Vi is also known as mucopolysaccharidosis vi, arylsulfatase b deficiency, mucopolysaccharidosis type vi, maroteaux lamy syndrome, mps vi, deficiency of n-acetylgalactosamine-4-sulfatase (disorder), n-acetylgalactosamine-4-sulfatase deficiency, maroteaux-lamy syndrome (disorder), mucopoly-saccharidosis type vi, maroteaux - lamy syndrome, polydystrophic dwarfism, arsb deficiency, malnutrition, mps6.