Research of Fabry Disease has been linked to Angiokeratoma, Kidney Diseases, Pain, Hypertrophy, Lysosomal Storage Diseases. The study of Fabry Disease has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Fabry Disease include Pathogenesis, Excretion, Glomerular Filtration, Lipid Storage, Localization. These pathways complement our catalog of research reagents for the study of Fabry Disease including antibodies and ELISA kits against GB3, GB, ARSA, CTH, ELF3.
Top Research Reagents
We have 1252 products for the study of Fabry Disease that can be applied to Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Fabry Disease is also known as fabry disease, alpha-galactosidase a deficiency, fabry's disease (disorder), angiokeratoma diffuse, alpha galactosidase deficiency, deficiency of melibiase, angiokeratoma, diffuse, fabry's disease, angiokeratoma, malnutrition.