Research of Pseudo-hurler Polydystrophy has been linked to Mucolipidoses, Type Ii Mucolipidosis, Mucopolysaccharidoses, Mucopolysaccharidosis I, Lysosomal Storage Diseases. The study of Pseudo-hurler Polydystrophy has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Pseudo-hurler Polydystrophy include Transport, Glycosylation, Localization, Excretion, Secretion. These pathways complement our catalog of research reagents for the study of Pseudo-hurler Polydystrophy including antibodies and ELISA kits against GNPTG, CTSD, ARSA, GLB1, GNPTAB.
Pseudo-hurler Polydystrophy 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 Pseudo-hurler Polydystrophy below!
For more information on how to use Laverne, please read the How to Guide.
We have 1181 products for the study of Pseudo-hurler Polydystrophy that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Pseudo-hurler Polydystrophy is also known as Mucolipidosis Iii, Mucolipidosis Iiia, Mucolipidosis Type Iii, Mucolipidosis, Type Iii, Pseudo Hurler Polydystrophy.
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