Research of Refsum Disease has been linked to Zellweger Syndrome, Adrenoleukodystrophy, Infantile Refsum Disease (disorder), Peroxisomal Disorders, Adrenoleukodystrophy, Neonatal. The study of Refsum Disease has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Refsum Disease include Pathogenesis, Localization, Protein Import, Transport, Fatty Acid Beta-oxidation. These pathways complement our catalog of research reagents for the study of Refsum Disease including antibodies and ELISA kits against CHONDRODYSPLASIA, PHYTANOYL-COA HYDROXYLASE, C22, ABCD1, CAT.
Refsum 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 Refsum Disease below!
For more information on how to use Laverne, please read the How to Guide.
We have 352 products for the study of Refsum Disease that can be applied to Flow Cytometry, Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Refsum Disease is also known as refsum disease, heredopathia atactica polyneuritiformis, adult refsum disease, hmsn type iv, disorder of cornification 11 (phytanic acid type), hereditary motor and sensory neuropathy type iv, herditary sensory and motor neuropathy type 4, hereditary motor and sensory neuropathy iv, hereditary motorsensory neuropathy iv, respiratory distress syndrome, adult, hypertrophic neuropathy of refsum, doc 11 (phytanic acid type), classic refsum disease, retinitis pigmentosa, inherited neuropathy, refsum's disease, hsmn iv, hmsn iv, hmsn 4, crd, ard.