Fabry Disease

Fabry disease (also known as alpha-galactosidase-A deficiency) is an inherited lysosomal storage disease that is caused by the lack of or faulty enzyme needed to metabolize lipids and fat-like substances. Research on Fabry Disease has focused on the targets listed below.

Important targets related to Fabry Disease

The following targets are directly related to research on Fabry Disease. Find Antibodies, Kits, Reagents and other products.