Research of Type I Mucolipidosis has been linked to Mucolipidoses, Neuraminidase 1 Deficiency, Myoclonus, Lysosomal Storage Diseases, Galactosialidosis. The study of Type I Mucolipidosis has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Type I Mucolipidosis include Excretion, Transport, Localization, Pathogenesis, Methylation. These pathways complement our catalog of research reagents for the study of Type I Mucolipidosis including antibodies and ELISA kits against GLB1, NEU1, CTSA, EGFL7, NEU3.
Type I Mucolipidosis 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 Type I Mucolipidosis below!
For more information on how to use Laverne, please read the How to Guide.
We have 1940 products for the study of Type I Mucolipidosis that can be applied to Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Type I Mucolipidosis is also known as Mucolipidosis Type I, Sialidoses, Sialidosis, Cherry Red Spot-myoclonus Syndrome, Cherry-red Spot Myoclonus Syndrome.