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 GLA, NAT8, ELF3, GB3, NAGA.
Fabry Disease 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 Fabry Disease below!
For more information on how to use Laverne, please read the How to Guide.
We have 663 products for the study of Fabry Disease that can be applied to Western Blot, Flow Cytometry, Immunohistochemistry, Chromatin Immunoprecipitation (ChIP), Immunocytochemistry/Immunofluorescence 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.
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