Research of Mucopolysaccharidosis I has been linked to Pfaundler-hurler Syndrome, Mucopolysaccharidoses, Mucopolysaccharidosis Ii, Lysosomal Storage Diseases, Mucopolysaccharidosis V. The study of Mucopolysaccharidosis I has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Mucopolysaccharidosis I include Excretion, Immune Response, Pathogenesis, Transport, Secretion. These pathways complement our catalog of research reagents for the study of Mucopolysaccharidosis I including antibodies and ELISA kits against ALPHA-L-IDURONIDASE, IDURONATE SULFATASE, ARSA, ARSB, CAT.
Mucopolysaccharidosis I 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 I below!
For more information on how to use Laverne, please read the How to Guide.
We have 658 products for the study of Mucopolysaccharidosis I that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Mucopolysaccharidosis I is also known as mucopolysaccharidosis i, mucopolysaccharidosis type i, idua deficiency, mps i, mps 1, scheie syndrome (former subtype, formerly known as mucopoly-saccharidosis type v), mucopolysaccharidosis, mps-i (disorder), hurler-scheie syndrome (former subtype), hurler syndrome (former subtype), iduronidase deficiency disease, mucopolysaccharidosis, type 1, attenuated mps i (subtype), pfaundler-hurler syndrome, mucopolysaccharidosis v, severe mps i (subtype), mucopolysaccharidoses, lipochondrodystrophy, hurler syndrome, scheie syndrome, malnutrition, mps1.